ENST00000366641.4:c.1108C>A
MANE Select
|
ENSP00000355601.3:p.Arg370Ser
|
|
ENST00000476717.2:n.385C>A
|
|
|
ENST00000653198.1:n.650C>A
|
|
|
ENST00000653908.1:c.151-2966C>A
|
ENSP00000499669.1:n.151-2966C>A
|
|
ENST00000654803.1:c.330C>A
|
|
|
ENST00000658954.1:c.482C>A
|
|
|
ENST00000662216.1:c.247C>A
|
ENSP00000499467.1:p.Arg83Ser
|
|
ENST00000663780.1:n.208C>A
|
|
|
ENST00000667629.1:c.316-2966C>A
|
ENSP00000499629.1:n.316-2966C>A
|
|
ENST00000670301.1:c.230-4127C>A
|
|
|
ENST00000366641.3:c.1108C>A
|
ENSP00000355601.3:p.Arg370Ser
|
|
ENST00000476717.1:n.385C>A
|
|
|
NM_022051.2:c.1108C>A
|
NP_071334.1:p.Arg370Ser
|
|
XM_005273166.3:c.1108C>A
|
XP_005273223.1:p.Arg370Ser
|
|
XM_005273167.3:c.1012-2966C>A
|
XP_005273224.1:n.1012-2966C>A
|
|
XM_005273166.5:c.1108C>A
|
XP_005273223.1:p.Arg370Ser
|
|
XM_005273167.5:c.1012-2966C>A
|
XP_005273224.1:n.1012-2966C>A
|
|
XM_024447734.1:c.1012-2966C>A
|
XP_024303502.1:n.1012-2966C>A
|
|
NM_001377260.1:c.1108C>A
|
NP_001364189.1:p.Arg370Ser
|
|
NM_001377261.1:c.1012-2966C>A
|
NP_001364190.1:n.1012-2966C>A
|
|
NM_022051.3:c.1108C>A
MANE Select
|
NP_071334.1:p.Arg370Ser
|
|