ENST00000347454.9:c.715G>C
MANE Select
|
ENSP00000233552.6:p.Asp239His
|
|
ENST00000347454.8:c.715G>C
|
ENSP00000233552.5:p.Asp239His
|
|
ENST00000405940.6:c.689G>C
|
ENSP00000384375.2:p.Gly230Ala
|
|
ENST00000417567.1:c.291G>C
|
|
|
ENST00000445933.6:c.712G>C
|
ENSP00000394397.2:p.Asp238His
|
|
ENST00000451130.6:c.775G>C
|
ENSP00000394869.2:p.Asp259His
|
|
ENST00000475582.5:n.2038G>C
|
|
|
ENST00000493344.6:c.778G>C
|
ENSP00000429323.1:p.Asp260His
|
|
ENST00000616081.4:c.706G>C
|
ENSP00000477710.1:p.Asp236His
|
|
ENST00000622434.4:c.670G>C
|
ENSP00000479991.1:p.Asp224His
|
|
NM_001034116.1:c.715G>C
|
NP_001029288.1:p.Asp239His
|
|
NM_015636.3:c.712G>C
|
NP_056451.3:p.Asp238His
|
|
NM_172195.3:c.775G>C
|
NP_751945.2:p.Asp259His
|
|
XM_005264632.1:c.670G>C
|
XP_005264689.1:p.Asp224His
|
|
XM_006712132.1:c.667G>C
|
XP_006712195.1:p.Asp223His
|
|
XM_011533147.1:c.97G>C
|
XP_011531449.1:p.Asp33His
|
|
NM_001318965.1:c.778G>C
|
NP_001305894.1:p.Asp260His
|
|
NM_001318966.1:c.670G>C
|
NP_001305895.1:p.Asp224His
|
|
NM_001318967.1:c.622G>C
|
NP_001305896.1:p.Asp208His
|
|
NM_001318968.1:c.130G>C
|
NP_001305897.1:p.Asp44His
|
|
NM_001318969.1:c.97G>C
|
NP_001305898.1:p.Asp33His
|
|
XM_011533147.2:c.97G>C
|
XP_011531449.1:p.Asp33His
|
|
NM_001034116.2:c.715G>C
MANE Select
|
NP_001029288.1:p.Asp239His
|
|
NM_001318965.2:c.778G>C
|
NP_001305894.1:p.Asp260His
|
|
NM_001318966.2:c.670G>C
|
NP_001305895.1:p.Asp224His
|
|
NM_001318967.2:c.622G>C
|
NP_001305896.1:p.Asp208His
|
|
NM_001318968.2:c.130G>C
|
NP_001305897.1:p.Asp44His
|
|
NM_001318969.2:c.97G>C
|
NP_001305898.1:p.Asp33His
|
|
NM_015636.4:c.712G>C
|
NP_056451.3:p.Asp238His
|
|
NM_172195.4:c.775G>C
|
NP_751945.2:p.Asp259His
|
|