ENST00000348931.9:c.422A>C
MANE Select
|
ENSP00000335384.5:p.Asp141Ala
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|
ENST00000348931.8:c.422A>C
|
ENSP00000335384.5:p.Asp141Ala
|
|
ENST00000377940.3:c.356A>C
|
ENSP00000367174.3:p.Asp119Ala
|
|
ENST00000583811.5:c.68A>C
|
ENSP00000462463.1:p.Asp23Ala
|
|
ENST00000584588.5:c.406+660A>C
|
ENSP00000462067.1:n.406+660A>C
|
|
NM_198844.2:c.356A>C
|
NP_942141.2:p.Asp119Ala
|
|
NM_199321.2:c.422A>C
|
NP_955353.1:p.Asp141Ala
|
|
XM_011524298.1:c.422A>C
|
XP_011522600.1:p.Asp141Ala
|
|
XR_002957959.1:n.613A>C
|
|
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NM_198844.3:c.356A>C
|
NP_942141.2:p.Asp119Ala
|
|
NM_199321.3:c.422A>C
MANE Select
|
NP_955353.1:p.Asp141Ala
|
|