ENST00000281928.9:c.2797T>G
MANE Select
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ENSP00000281928.3:p.Ser933Ala
|
|
ENST00000548743.2:c.2767T>G
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ENSP00000448553.2:p.Ser923Ala
|
|
ENST00000549786.2:c.2225T>G
|
|
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ENST00000647927.1:n.3170T>G
|
|
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ENST00000648173.1:n.1592T>G
|
|
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ENST00000648379.1:n.1165T>G
|
|
|
ENST00000648737.1:n.2561T>G
|
|
|
ENST00000648916.1:n.808T>G
|
|
|
ENST00000649607.1:c.981T>G
|
|
|
ENST00000650226.1:c.2797T>G
|
ENSP00000496981.1:p.Ser933Ala
|
|
ENST00000281928.7:c.2797T>G
|
ENSP00000281928.3:p.Ser933Ala
|
|
NM_015335.4:c.2797T>G
|
NP_056150.1:p.Ser933Ala
|
|
XM_011538080.1:c.2797T>G
|
XP_011536382.1:p.Ser933Ala
|
|
XM_011538081.1:c.2794T>G
|
XP_011536383.1:p.Ser932Ala
|
|
XM_011538082.1:c.2767T>G
|
XP_011536384.1:p.Ser923Ala
|
|
XM_011538080.2:c.2797T>G
|
XP_011536382.1:p.Ser933Ala
|
|
XM_011538081.2:c.2794T>G
|
XP_011536383.1:p.Ser932Ala
|
|
XM_011538082.2:c.2767T>G
|
XP_011536384.1:p.Ser923Ala
|
|
XM_017019090.1:c.2794T>G
|
XP_016874579.1:p.Ser932Ala
|
|
NM_015335.5:c.2797T>G
MANE Select
|
NP_056150.1:p.Ser933Ala
|
|