ENST00000350026.11:c.2775A>G
|
ENSP00000055163.8:p.Arg925=
|
|
ENST00000414678.8:c.2685A>G
|
ENSP00000412835.3:p.Arg895=
|
|
ENST00000637015.2:c.2775A>G
|
ENSP00000489729.2:p.Arg925=
|
|
ENST00000319584.11:c.789A>G
|
ENSP00000313006.7:p.Arg263=
|
|
ENST00000346085.10:c.2814A>G
|
ENSP00000344546.5:p.Arg938=
|
|
ENST00000350026.10:c.2526A>G
|
ENSP00000055163.7:p.Arg842=
|
|
ENST00000414678.7:c.933A>G
|
ENSP00000412835.2:p.Arg311=
|
|
ENST00000452544.2:n.676A>G
|
|
|
ENST00000635849.1:c.96A>G
|
ENSP00000490948.1:p.Arg32=
|
|
ENST00000636930.2:c.2775A>G
MANE Select
|
ENSP00000490491.2:p.Arg925=
|
|
ENST00000637015.1:c.14A>G
|
|
|
ENST00000637810.1:c.276A>G
|
ENSP00000489636.1:p.Arg92=
|
|
ENST00000637904.1:c.276A>G
|
ENSP00000490550.1:p.Arg92=
|
|
ENST00000647938.1:c.2565A>G
|
ENSP00000498155.1:p.Arg855=
|
|
ENST00000674190.1:n.1524A>G
|
|
|
ENST00000319584.10:c.792A>G
|
ENSP00000313006.6:p.Arg264=
|
|
ENST00000346085.9:c.2565A>G
|
ENSP00000344546.4:p.Arg855=
|
|
ENST00000350026.9:c.2526A>G
|
ENSP00000055163.7:p.Arg842=
|
|
ENST00000414678.6:c.933A>G
|
ENSP00000412835.2:p.Arg311=
|
|
ENST00000452544.1:n.622A>G
|
|
|
NM_017519.2:c.2526A>G
|
NP_059989.2:p.Arg842=
|
|
NM_020732.3:c.2565A>G
|
NP_065783.3:p.Arg855=
|
|
XM_005267069.3:c.2526A>G
|
XP_005267126.2:p.Arg842=
|
|
XM_011535984.1:c.1476A>G
|
XP_011534286.1:p.Arg492=
|
|
XM_011535985.1:c.1296A>G
|
XP_011534287.1:p.Arg432=
|
|
XM_011535986.1:c.1056A>G
|
XP_011534288.1:p.Arg352=
|
|
XM_011535987.1:c.675A>G
|
XP_011534289.1:p.Arg225=
|
|
XM_011535988.1:c.-20+15430A>G
|
XP_011534290.1:n.-20+15430A>G
|
|
NM_001346813.1:c.2526A>G
|
NP_001333742.1:p.Arg842=
|
|
NM_001363725.1:c.276A>G
|
NP_001350654.1:p.Arg92=
|
|
XM_011535984.2:c.2607A>G
|
XP_011534286.2:p.Arg869=
|
|
XM_011535988.3:c.-20+15430A>G
|
XP_011534290.1:n.-20+15430A>G
|
|
XM_017011103.2:c.2607A>G
|
XP_016866592.1:p.Arg869=
|
|
XM_017011104.1:c.2607A>G
|
XP_016866593.1:p.Arg869=
|
|
XM_017011105.2:c.2607A>G
|
XP_016866594.1:p.Arg869=
|
|
XM_017011106.2:c.2607A>G
|
XP_016866595.1:p.Arg869=
|
|
XM_017011107.2:c.2427A>G
|
XP_016866596.1:p.Arg809=
|
|
XR_002956289.1:n.2690A>G
|
|
|
NM_001363725.2:c.276A>G
|
NP_001350654.1:p.Arg92=
|
|
NM_001371656.1:c.2814A>G
|
NP_001358585.1:p.Arg938=
|
|
NM_001374820.1:c.2814A>G
|
NP_001361749.1:p.Arg938=
|
|
NM_001374828.1:c.2775A>G
MANE Select
|
NP_001361757.1:p.Arg925=
|
|
NM_017519.3:c.2775A>G
|
NP_059989.3:p.Arg925=
|
|