ENST00000622290.5:c.3698T>C
|
ENSP00000483331.2:p.Val1233Ala
|
|
ENST00000205557.12:c.3698T>C
MANE Select
|
ENSP00000205557.7:p.Val1233Ala
|
|
ENST00000640696.1:c.512T>C
|
ENSP00000492197.1:p.Val171Ala
|
|
ENST00000205557.11:c.3698T>C
|
ENSP00000205557.7:p.Val1233Ala
|
|
ENST00000456970.6:c.3323T>C
|
ENSP00000405002.2:n.3323T>C
|
|
ENST00000622290.4:c.*907T>C
|
ENSP00000483331.1:n.*907T>C
|
|
NM_001171.5:c.3698T>C
|
NP_001162.4:p.Val1233Ala
|
|
XM_011522479.1:c.3665T>C
|
XP_011520781.1:p.Val1222Ala
|
|
XM_011522480.1:c.3356T>C
|
XP_011520782.1:p.Val1119Ala
|
|
XM_011522481.1:c.3356T>C
|
XP_011520783.1:p.Val1119Ala
|
|
XR_932836.1:n.3933T>C
|
|
|
XR_932837.1:n.3734T>C
|
|
|
XR_932838.1:n.3734T>C
|
|
|
XR_933134.1:n.539-262A>G
|
|
|
NM_001351800.1:c.3356T>C
|
NP_001338729.1:p.Val1119Ala
|
|
NR_147784.1:n.3360T>C
|
|
|
XM_011522479.2:c.3665T>C
|
XP_011520781.1:p.Val1222Ala
|
|
XM_011522481.3:c.3356T>C
|
XP_011520783.1:p.Val1119Ala
|
|
XM_017023212.1:c.3530T>C
|
XP_016878701.1:p.Val1177Ala
|
|
XM_024450261.1:c.3734T>C
|
XP_024306029.1:p.Val1245Ala
|
|
XR_932836.2:n.3879T>C
|
|
|
XR_932837.3:n.3679T>C
|
|
|
XR_932838.3:n.3679T>C
|
|
|
NM_001171.6:c.3698T>C
MANE Select
|
NP_001162.5:p.Val1233Ala
|
|