ENST00000225927.7:c.1426A>T
MANE Select
|
ENSP00000225927.1:p.Thr476Ser
|
|
ENST00000225927.6:c.1426A>T
|
ENSP00000225927.1:p.Thr476Ser
|
|
ENST00000591587.1:c.764A>T
|
ENSP00000467836.1:n.764A>T
|
|
ENST00000592454.1:c.465A>T
|
|
|
NM_000263.3:c.1426A>T
|
NP_000254.2:p.Thr476Ser
|
|
XM_006721920.2:c.595A>T
|
XP_006721983.1:p.Thr199Ser
|
|
XM_011524840.1:c.427A>T
|
XP_011523142.1:p.Thr143Ser
|
|
XM_017024687.1:c.595A>T
|
XP_016880176.1:p.Thr199Ser
|
|
XM_024450771.1:c.1483A>T
|
XP_024306539.1:p.Thr495Ser
|
|
XM_024450772.1:c.427A>T
|
XP_024306540.1:p.Thr143Ser
|
|
NM_000263.4:c.1426A>T
MANE Select
|
NP_000254.2:p.Thr476Ser
|
|