ENST00000261819.8:c.1715A=
MANE Select
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ENSP00000261819.3:p.Gln572=
|
|
ENST00000261819.7:c.1715A=
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ENSP00000261819.3:p.Gln572=
|
|
ENST00000441917.6:c.1379A=
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ENSP00000415061.2:p.Gln460=
|
|
ENST00000534976.5:n.2371A=
|
|
|
ENST00000535482.1:c.713A=
|
ENSP00000438754.1:p.Gln238=
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|
ENST00000535641.5:n.1926A=
|
|
|
ENST00000539079.5:c.1059A=
|
|
|
ENST00000541887.5:c.1676A=
|
ENSP00000439875.1:p.Gln559=
|
|
ENST00000544314.5:n.833A=
|
|
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ENST00000545218.5:n.958A=
|
|
|
NM_001137559.1:c.1379A=
|
NP_001131031.1:p.Gln460=
|
|
NM_016237.4:c.1715A=
|
NP_057321.2:p.Gln572=
|
|
XM_005253900.2:c.1676A=
|
XP_005253957.1:p.Gln559=
|
|
XM_006719449.1:c.521A=
|
XP_006719512.1:p.Gln174=
|
|
NM_001330489.1:c.1676A=
|
NP_001317418.1:p.Gln559=
|
|
XM_017019423.2:c.521A=
|
XP_016874912.1:p.Gln174=
|
|
XM_017019424.2:c.521A=
|
XP_016874913.1:p.Gln174=
|
|
NM_016237.5:c.1715A=
MANE Select
|
NP_057321.2:p.Gln572=
|
|
NM_001330489.2:c.1676A=
|
NP_001317418.1:p.Gln559=
|
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