ENST00000399503.4:c.822T>C
MANE Select
|
ENSP00000382423.3:p.Val274=
|
|
ENST00000399503.3:c.822T>C
|
ENSP00000382423.3:p.Val274=
|
|
NM_005921.1:c.822T>C
|
NP_005912.1:p.Val274=
|
|
XM_005248519.3:c.444T>C
|
XP_005248576.2:p.Val148=
|
|
XM_011543406.1:c.567T>C
|
XP_011541708.1:p.Val189=
|
|
XM_011543407.1:c.822T>C
|
XP_011541709.1:p.Val274=
|
|
XM_011543408.1:c.822T>C
|
XP_011541710.1:p.Val274=
|
|
XM_017009484.1:c.411T>C
|
XP_016864973.1:p.Val137=
|
|
XM_017009485.1:c.333T>C
|
XP_016864974.1:p.Val111=
|
|
XR_001742068.2:n.853T>C
|
|
|
NM_005921.2:c.822T>C
MANE Select
|
NP_005912.1:p.Val274=
|
|