ENST00000219070.9:c.1299G>A
MANE Select
|
ENSP00000219070.4:p.Leu433=
|
|
ENST00000219070.8:c.1299G>A
|
ENSP00000219070.4:p.Leu433=
|
|
ENST00000437642.6:c.1149G>A
|
ENSP00000394237.2:p.Leu383=
|
|
ENST00000543485.5:c.1071G>A
|
ENSP00000444143.1:p.Leu357=
|
|
ENST00000570283.1:c.174G>A
|
ENSP00000456518.1:p.Leu58=
|
|
ENST00000570308.5:c.1071G>A
|
ENSP00000461421.1:p.Leu357=
|
|
NM_001127891.2:c.1149G>A
|
NP_001121363.1:p.Leu383=
|
|
NM_001302508.1:c.1071G>A
|
NP_001289437.1:p.Leu357=
|
|
NM_001302509.1:c.1071G>A
|
NP_001289438.1:p.Leu357=
|
|
NM_001302510.1:c.1071G>A
|
NP_001289439.1:p.Leu357=
|
|
NM_004530.5:c.1299G>A
|
NP_004521.1:p.Leu433=
|
|
NM_004530.6:c.1299G>A
MANE Select
|
NP_004521.1:p.Leu433=
|
|
NM_001127891.3:c.1149G>A
|
NP_001121363.1:p.Leu383=
|
|
NM_001302509.2:c.1071G>A
|
NP_001289438.1:p.Leu357=
|
|
NM_001302510.2:c.1071G>A
|
NP_001289439.1:p.Leu357=
|
|