ENST00000223051.8:c.728G>T
MANE Select
|
ENSP00000223051.3:p.Gly243Val
|
|
ENST00000223051.7:c.728G>T
|
ENSP00000223051.3:p.Gly243Val
|
|
ENST00000431692.5:c.728G>T
|
ENSP00000413905.1:p.Gly243Val
|
|
ENST00000462107.1:c.728G>T
|
ENSP00000420525.1:p.Gly243Val
|
|
ENST00000465294.5:n.733G>T
|
|
|
ENST00000473374.5:n.178G>T
|
|
|
ENST00000473571.1:n.182G>T
|
|
|
ENST00000475011.1:n.257G>T
|
|
|
ENST00000476304.5:n.349G>T
|
|
|
NM_001206855.1:c.215G>T
|
NP_001193784.1:p.Gly72Val
|
|
NM_003227.3:c.728G>T
|
NP_003218.2:p.Gly243Val
|
|
XM_005250553.3:c.728G>T
|
XP_005250610.1:p.Gly243Val
|
|
XM_005250554.3:c.728G>T
|
XP_005250611.1:p.Gly243Val
|
|
NM_001206855.2:c.215G>T
|
NP_001193784.1:p.Gly72Val
|
|
XM_005250553.4:c.728G>T
|
XP_005250610.1:p.Gly243Val
|
|
XM_017012573.1:c.728G>T
|
XP_016868062.1:p.Gly243Val
|
|
NM_003227.4:c.728G>T
MANE Select
|
NP_003218.2:p.Gly243Val
|
|
NM_001206855.3:c.215G>T
|
NP_001193784.1:p.Gly72Val
|
|