|
ENST00000392179.5:c.1179A>G
|
ENSP00000376018.4:p.Pro393=
|
|
|
ENST00000465923.6:n.830A>G
|
|
|
|
ENST00000467295.6:n.1707A>G
|
|
|
|
ENST00000468828.6:n.1006A>G
|
|
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ENST00000480762.6:n.1409A>G
|
|
|
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ENST00000483804.6:n.691A>G
|
|
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ENST00000493849.6:n.2034A>G
|
|
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|
ENST00000496553.6:n.1918A>G
|
|
|
|
ENST00000676535.1:n.1661A>G
|
|
|
|
ENST00000676583.1:c.*650A>G
|
ENSP00000503681.1:n.*650A>G
|
|
|
ENST00000676600.1:c.1179A>G
|
ENSP00000503989.1:p.Pro393=
|
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|
ENST00000676653.1:n.1935A>G
|
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|
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ENST00000676726.1:n.1608A>G
|
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ENST00000676770.1:n.2045A>G
|
|
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|
ENST00000676795.1:c.*761A>G
|
ENSP00000504650.1:n.*761A>G
|
|
|
ENST00000676871.1:n.1718A>G
|
|
|
|
ENST00000676972.1:c.1179A>G
MANE Select
|
ENSP00000503117.1:p.Pro393=
|
|
|
ENST00000676991.1:n.1769A>G
|
|
|
|
ENST00000677033.1:n.2248A>G
|
|
|
|
ENST00000677045.1:c.*850A>G
|
ENSP00000504168.1:n.*850A>G
|
|
|
ENST00000677050.1:n.1833A>G
|
|
|
|
ENST00000677063.1:c.*850A>G
|
ENSP00000504572.1:n.*850A>G
|
|
|
ENST00000677081.1:c.*111A>G
|
ENSP00000503728.1:n.*111A>G
|
|
|
ENST00000677089.1:n.2733A>G
|
|
|
|
ENST00000677103.1:n.1644A>G
|
|
|
|
ENST00000677138.1:c.*156A>G
|
ENSP00000504839.1:n.*156A>G
|
|
|
ENST00000677178.1:n.1482A>G
|
|
|
|
ENST00000677231.1:c.1101A>G
|
ENSP00000503378.1:p.Pro367=
|
|
|
ENST00000677336.1:n.1533A>G
|
|
|
|
ENST00000677350.1:n.1977A>G
|
|
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|
ENST00000677358.1:n.1272A>G
|
|
|
|
ENST00000677383.1:n.2645A>G
|
|
|
|
ENST00000677453.1:c.1242A>G
|
ENSP00000503604.1:p.Pro414=
|
|
|
ENST00000677457.1:c.1179A>G
|
ENSP00000503294.1:p.Pro393=
|
|
|
ENST00000677471.1:n.1533A>G
|
|
|
|
ENST00000677495.1:n.1539A>G
|
|
|
|
ENST00000677547.1:c.*253A>G
|
ENSP00000504269.1:n.*253A>G
|
|
|
ENST00000677550.1:c.1179A>G
|
ENSP00000503353.1:p.Pro393=
|
|
|
ENST00000677577.1:n.3674A>G
|
|
|
|
ENST00000677579.1:c.1242A>G
|
ENSP00000504162.1:p.Pro414=
|
|
|
ENST00000677613.1:c.*111A>G
|
ENSP00000504258.1:n.*111A>G
|
|
|
ENST00000677643.1:n.1588A>G
|
|
|
|
ENST00000677653.1:c.*554A>G
|
ENSP00000504542.1:n.*554A>G
|
|
|
ENST00000677657.1:n.1588A>G
|
|
|
|
ENST00000677736.1:n.1833A>G
|
|
|
|
ENST00000677745.1:n.1992A>G
|
|
|
|
ENST00000677807.1:n.1798A>G
|
|
|
|
ENST00000677809.1:n.1977A>G
|
|
|
|
ENST00000677837.1:c.*913A>G
|
ENSP00000503661.1:n.*913A>G
|
|
|
ENST00000677846.1:c.1242A>G
|
ENSP00000504065.1:p.Pro414=
|
|
|
ENST00000677916.1:n.3358A>G
|
|
|
|
ENST00000677925.1:n.1798A>G
|
|
|
|
ENST00000677948.1:c.*864A>G
|
ENSP00000503510.1:n.*864A>G
|
|
|
ENST00000678052.1:n.2560A>G
|
|
|
|
ENST00000678068.1:n.2910A>G
|
|
|
|
ENST00000678130.1:n.1890A>G
|
|
|
|
ENST00000678328.1:n.1904A>G
|
|
|
|
ENST00000678356.1:n.3254A>G
|
|
|
|
ENST00000678484.1:n.3674A>G
|
|
|
|
ENST00000678492.1:n.3438A>G
|
|
|
|
ENST00000678507.1:c.1179A>G
|
ENSP00000504199.1:p.Pro393=
|
|
|
ENST00000678511.1:c.1179A>G
|
ENSP00000504846.1:p.Pro393=
|
|
|
ENST00000678532.1:c.*864A>G
|
ENSP00000504682.1:n.*864A>G
|
|
|
ENST00000678559.1:c.*973A>G
|
ENSP00000504285.1:n.*973A>G
|
|
|
ENST00000678605.1:c.1179A>G
|
ENSP00000503969.1:p.Pro393=
|
|
|
ENST00000678613.1:n.3438A>G
|
|
|
|
ENST00000678648.1:n.1849A>G
|
|
|
|
ENST00000678783.1:c.1104A>G
|
ENSP00000504215.1:p.Pro368=
|
|
|
ENST00000678793.1:c.*502A>G
|
ENSP00000503431.1:n.*502A>G
|
|
|
ENST00000678850.1:n.1539A>G
|
|
|
|
ENST00000678880.1:c.*720A>G
|
ENSP00000503015.1:n.*720A>G
|
|
|
ENST00000678911.1:c.1101A>G
|
ENSP00000503946.1:p.Pro367=
|
|
|
ENST00000678966.1:n.1597A>G
|
|
|
|
ENST00000678982.1:c.*850A>G
|
ENSP00000504597.1:n.*850A>G
|
|
|
ENST00000679064.1:c.*44A>G
|
ENSP00000502868.1:n.*44A>G
|
|
|
ENST00000679071.1:n.1711A>G
|
|
|
|
ENST00000679142.1:c.1279A>G
|
ENSP00000504800.1:n.1279A>G
|
|
|
ENST00000679169.1:c.*943A>G
|
ENSP00000504096.1:n.*943A>G
|
|
|
ENST00000679176.1:c.1179A>G
|
ENSP00000504170.1:p.Pro393=
|
|
|
ENST00000679215.1:n.2073A>G
|
|
|
|
ENST00000679239.1:c.*554A>G
|
ENSP00000504555.1:n.*554A>G
|
|
|
ENST00000679282.1:c.*44A>G
|
ENSP00000504533.1:n.*44A>G
|
|
|
ENST00000367993.7:c.1179A>G
|
ENSP00000356972.3:p.Pro393=
|
|
|
ENST00000392179.4:c.1179A>G
|
ENSP00000376018.4:p.Pro393=
|
|
|
ENST00000465923.5:n.544A>G
|
|
|
|
ENST00000468828.5:n.286A>G
|
|
|
|
ENST00000483804.5:n.803A>G
|
|
|
|
ENST00000492153.1:n.193A>G
|
|
|
|
ENST00000493849.5:n.229A>G
|
|
|
|
NM_001166159.1:c.1179A>G
|
NP_001159631.1:p.Pro393=
|
|
|
NM_004550.4:c.1179A>G
|
NP_004541.1:p.Pro393=
|
|
|
XM_005245208.1:c.1179A>G
|
XP_005245265.1:p.Pro393=
|
|
|
XM_005245209.1:c.885A>G
|
XP_005245266.1:p.Pro295=
|
|
|
XM_005245209.2:c.885A>G
|
XP_005245266.1:p.Pro295=
|
|
|
NM_001166159.2:c.1179A>G
|
NP_001159631.1:p.Pro393=
|
|
|
NM_001377298.1:c.1179A>G
|
NP_001364227.1:p.Pro393=
|
|
|
NM_001377299.1:c.1179A>G
MANE Select
|
NP_001364228.1:p.Pro393=
|
|
|
NM_001377300.1:c.1179A>G
|
NP_001364229.1:p.Pro393=
|
|
|
NM_001377301.1:c.1179A>G
|
NP_001364230.1:p.Pro393=
|
|
|
NM_001377302.1:c.1179A>G
|
NP_001364231.1:p.Pro393=
|
|
|
NR_165188.1:n.1068A>G
|
|
|
|
NM_004550.5:c.1179A>G
|
NP_004541.1:p.Pro393=
|
|
