ENST00000321612.8:c.2056G>T
MANE Select
|
ENSP00000370737.4:p.Asp686Tyr
|
|
ENST00000638233.1:n.491G>T
|
|
|
ENST00000638661.1:c.256G>T
|
ENSP00000491369.1:p.Asp86Tyr
|
|
ENST00000638694.1:n.243G>T
|
|
|
ENST00000639318.1:c.256G>T
|
ENSP00000491932.1:p.Asp86Tyr
|
|
ENST00000639364.1:n.1756G>T
|
|
|
ENST00000639443.1:n.1624G>T
|
|
|
ENST00000639954.1:n.1764G>T
|
|
|
ENST00000640505.1:n.295G>T
|
|
|
ENST00000321612.6:c.2056G>T
|
ENSP00000370737.3:p.Asp686Tyr
|
|
NM_000170.2:c.2056G>T , LRG_643t1:c.2056G>T
|
NP_000161.2:p.Asp686Tyr
|
|
NM_000170.3:c.2056G>T
MANE Select
|
NP_000161.2:p.Asp686Tyr
|
|