ENST00000642418.1:n.1549G>T
|
|
|
ENST00000643693.1:n.1013G>T
|
|
|
ENST00000644795.1:c.1003G>T
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ENSP00000495720.1:p.Ala335Ser
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|
ENST00000646782.1:n.1945G>T
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|
|
ENST00000647165.2:c.9211G>T
MANE Select
|
ENSP00000495481.1:p.Ala3071Ser
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ENST00000651214.1:n.1716G>T
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|
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ENST00000205890.9:c.9211G>T
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ENSP00000205890.5:p.Ala3071Ser
|
|
ENST00000418233.7:c.1003G>T
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ENSP00000408800.3:p.Ala335Ser
|
|
ENST00000433411.7:n.148G>T
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|
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ENST00000445289.6:n.316+1429G>T
|
|
|
ENST00000556535.5:c.73G>T
|
ENSP00000451782.1:p.Ala25Ser
|
|
ENST00000557190.5:n.113G>T
|
|
|
ENST00000557655.5:c.73G>T
|
ENSP00000451925.1:p.Ala25Ser
|
|
ENST00000578472.5:c.73G>T
|
ENSP00000467989.1:p.Ala25Ser
|
|
ENST00000615845.4:c.9211G>T
|
ENSP00000481642.1:p.Ala3071Ser
|
|
NM_016239.3:c.9211G>T
|
NP_057323.3:p.Ala3071Ser
|
|
XM_011523921.1:c.9205G>T
|
XP_011522223.1:p.Ala3069Ser
|
|
XM_017024714.2:c.9151G>T
|
XP_016880203.1:p.Ala3051Ser
|
|
XM_017024715.2:c.9214G>T
|
XP_016880204.1:p.Ala3072Ser
|
|
NM_016239.4:c.9211G>T
MANE Select
|
NP_057323.3:p.Ala3071Ser
|
|