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ENST00000375687.10:c.4094G>C
MANE Select
|
ENSP00000364839.4:p.Gly1365Ala
|
|
|
ENST00000646985.1:c.3911G>C
|
ENSP00000495053.1:p.Gly1304Ala
|
|
|
ENST00000647223.1:n.6447G>C
|
|
|
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ENST00000651418.1:c.1870-1624G>C
|
ENSP00000499150.1:n.1870-1624G>C
|
|
|
ENST00000306058.9:c.4079G>C
|
ENSP00000305119.5:p.Gly1360Ala
|
|
|
ENST00000375687.8:c.4094G>C
|
ENSP00000364839.4:p.Gly1365Ala
|
|
|
ENST00000613218.4:c.4094G>C
|
ENSP00000480487.1:p.Gly1365Ala
|
|
|
ENST00000620121.4:c.4094G>C
|
ENSP00000481978.1:p.Gly1365Ala
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|
|
NM_015338.5:c.4094G>C , LRG_630t1:c.4094G>C
|
NP_056153.2:p.Gly1365Ala
|
|
|
XM_006723727.2:c.4091G>C
|
XP_006723790.1:p.Gly1364Ala
|
|
|
XM_006723728.2:c.4064G>C
|
XP_006723791.1:p.Gly1355Ala
|
|
|
XM_006723730.2:c.4010G>C
|
XP_006723793.1:p.Gly1337Ala
|
|
|
XM_006723732.2:c.3911G>C
|
XP_006723795.1:p.Gly1304Ala
|
|
|
XM_006723733.1:c.3410G>C
|
XP_006723796.1:p.Gly1137Ala
|
|
|
XM_011528647.1:c.4358G>C
|
XP_011526949.1:p.Gly1453Ala
|
|
|
XM_011528648.1:c.4355G>C
|
XP_011526950.1:p.Gly1452Ala
|
|
|
XM_011528649.1:c.4274G>C
|
XP_011526951.1:p.Gly1425Ala
|
|
|
XM_011528650.1:c.4205G>C
|
XP_011526952.1:p.Gly1402Ala
|
|
|
XM_011528651.1:c.4073G>C
|
XP_011526953.1:p.Gly1358Ala
|
|
|
XM_011528652.1:c.4010G>C
|
XP_011526954.1:p.Gly1337Ala
|
|
|
NM_001363734.1:c.3911G>C
|
NP_001350663.1:p.Gly1304Ala
|
|
|
XM_006723727.3:c.4091G>C
|
XP_006723790.1:p.Gly1364Ala
|
|
|
XM_006723728.3:c.4064G>C
|
XP_006723791.1:p.Gly1355Ala
|
|
|
XM_006723730.4:c.4010G>C
|
XP_006723793.1:p.Gly1337Ala
|
|
|
XM_011528648.3:c.4355G>C
|
XP_011526950.1:p.Gly1452Ala
|
|
|
XM_011528652.2:c.4010G>C
|
XP_011526954.1:p.Gly1337Ala
|
|
|
XM_017027704.1:c.4010G>C
|
XP_016883193.1:p.Gly1337Ala
|
|
|
XM_017027705.1:c.4010G>C
|
XP_016883194.1:p.Gly1337Ala
|
|
|
XM_017027706.1:c.3941G>C
|
XP_016883195.1:p.Gly1314Ala
|
|
|
NM_015338.6:c.4094G>C
MANE Select
|
NP_056153.2:p.Gly1365Ala
|
|
