ENST00000302068.9:c.1068T>C
MANE Select
|
ENSP00000306099.4:p.Tyr356=
|
|
ENST00000302068.8:c.1068T>C
|
ENSP00000306099.4:p.Tyr356=
|
|
ENST00000502545.5:n.939+316T>C
|
|
|
ENST00000509493.1:c.411T>C
|
ENSP00000426757.1:p.Tyr137=
|
|
NM_001184741.1:c.891T>C
|
NP_001171670.1:p.Tyr297=
|
|
NM_005141.4:c.1068T>C , LRG_558t1:c.1068T>C
|
NP_005132.2:p.Tyr356=
|
|
NM_001382759.1:c.936T>C
|
NP_001369688.1:p.Tyr312=
|
|
NM_001382760.1:c.1068T>C
|
NP_001369689.1:p.Tyr356=
|
|
NM_001382761.1:c.1068T>C
|
NP_001369690.1:p.Tyr356=
|
|
NM_001382762.1:c.768T>C
|
NP_001369691.1:p.Tyr256=
|
|
NM_001382763.1:c.1059T>C
|
NP_001369692.1:p.Tyr353=
|
|
NM_001382764.1:c.1068T>C
|
NP_001369693.1:p.Tyr356=
|
|
NM_001382765.1:c.1068T>C
|
NP_001369694.1:p.Tyr356=
|
|
NM_005141.5:c.1068T>C
MANE Select
|
NP_005132.2:p.Tyr356=
|
|