ENST00000367049.9:c.6383G>T
MANE Select
|
ENSP00000356016.4:p.Ser2128Ile
|
|
ENST00000367051.6:c.5033G>T
|
ENSP00000356018.1:p.Ser1678Ile
|
|
ENST00000367052.6:c.5033G>T
|
ENSP00000356019.1:p.Ser1678Ile
|
|
ENST00000367053.6:c.5033G>T
|
ENSP00000356020.1:p.Ser1678Ile
|
|
ENST00000400960.7:c.5033G>T
|
ENSP00000383744.2:p.Ser1678Ile
|
|
ENST00000367049.8:c.6383G>T
|
ENSP00000356016.4:p.Ser2128Ile
|
|
ENST00000367051.5:c.5033G>T
|
ENSP00000356018.1:p.Ser1678Ile
|
|
ENST00000367052.5:c.5033G>T
|
ENSP00000356019.1:p.Ser1678Ile
|
|
ENST00000367053.5:c.5033G>T
|
ENSP00000356020.1:p.Ser1678Ile
|
|
ENST00000400960.6:c.5033G>T
|
ENSP00000383744.2:p.Ser1678Ile
|
|
ENST00000529814.1:c.1180-4811G>T
|
|
|
NM_000573.3:c.5033G>T
|
NP_000564.2:p.Ser1678Ile
|
|
NM_000651.4:c.6383G>T
|
NP_000642.3:p.Ser2128Ile
|
|
XM_006711166.2:c.6398G>T
|
XP_006711229.1:p.Ser2133Ile
|
|
XM_011509205.1:c.6398G>T
|
XP_011507507.1:p.Ser2133Ile
|
|
NM_000651.5:c.6383G>T
|
NP_000642.3:p.Ser2128Ile
|
|
XM_024453287.1:c.5048G>T
|
XP_024309055.1:p.Ser1683Ile
|
|
NM_000573.4:c.5033G>T
|
NP_000564.2:p.Ser1678Ile
|
|
NM_000651.6:c.6383G>T
MANE Select
|
NP_000642.3:p.Ser2128Ile
|
|