ENST00000223051.8:c.772G>C
MANE Select
|
ENSP00000223051.3:p.Asp258His
|
|
ENST00000223051.7:c.772G>C
|
ENSP00000223051.3:p.Asp258His
|
|
ENST00000431692.5:c.772G>C
|
ENSP00000413905.1:p.Asp258His
|
|
ENST00000462090.5:n.13G>C
|
|
|
ENST00000462107.1:c.772G>C
|
ENSP00000420525.1:p.Asp258His
|
|
ENST00000465294.5:n.777G>C
|
|
|
ENST00000473374.5:n.222G>C
|
|
|
ENST00000473571.1:n.226G>C
|
|
|
ENST00000475011.1:n.301G>C
|
|
|
ENST00000476304.5:n.393G>C
|
|
|
ENST00000490084.5:c.27G>C
|
|
|
NM_001206855.1:c.259G>C
|
NP_001193784.1:p.Asp87His
|
|
NM_003227.3:c.772G>C
|
NP_003218.2:p.Asp258His
|
|
XM_005250553.3:c.772G>C
|
XP_005250610.1:p.Asp258His
|
|
XM_005250554.3:c.772G>C
|
XP_005250611.1:p.Asp258His
|
|
NM_001206855.2:c.259G>C
|
NP_001193784.1:p.Asp87His
|
|
XM_005250553.4:c.772G>C
|
XP_005250610.1:p.Asp258His
|
|
XM_017012573.1:c.772G>C
|
XP_016868062.1:p.Asp258His
|
|
NM_003227.4:c.772G>C
MANE Select
|
NP_003218.2:p.Asp258His
|
|
NM_001206855.3:c.259G>C
|
NP_001193784.1:p.Asp87His
|
|