ENST00000377833.10:c.10743C>A
MANE Select
|
ENSP00000367064.4:p.Ser3581=
|
|
ENST00000377833.8:c.10743C>A
|
ENSP00000367064.4:p.Ser3581=
|
|
NM_001081.3:c.10743C>A , LRG_540t1:c.10743C>A
|
NP_001072.2:p.Ser3581=
|
|
XM_011519709.1:c.6729C>A
|
XP_011518011.1:p.Ser2243=
|
|
XM_011519710.1:c.6705C>A
|
XP_011518012.1:p.Ser2235=
|
|
XM_011519711.1:c.6585C>A
|
XP_011518013.1:p.Ser2195=
|
|
XM_011519709.2:c.6729C>A
|
XP_011518011.1:p.Ser2243=
|
|
XM_011519710.2:c.6705C>A
|
XP_011518012.1:p.Ser2235=
|
|
XM_011519711.3:c.6585C>A
|
XP_011518013.1:p.Ser2195=
|
|
NM_001081.4:c.10743C>A
MANE Select
|
NP_001072.2:p.Ser3581=
|
|