ENST00000350026.11:c.3762T>C
|
ENSP00000055163.8:p.Ala1254=
|
|
ENST00000414678.8:c.3831T>C
|
ENSP00000412835.3:p.Ala1277=
|
|
ENST00000637015.2:c.4050T>C
|
ENSP00000489729.2:p.Ala1350=
|
|
ENST00000346085.10:c.3801T>C
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ENSP00000344546.5:p.Ala1267=
|
|
ENST00000350026.10:c.3513T>C
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ENSP00000055163.7:p.Ala1171=
|
|
ENST00000414678.7:c.2079T>C
|
ENSP00000412835.2:p.Ala693=
|
|
ENST00000635849.1:c.1242T>C
|
ENSP00000490948.1:p.Ala414=
|
|
ENST00000635957.1:c.876T>C
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ENSP00000490385.1:p.Ala292=
|
|
ENST00000636930.2:c.3921T>C
MANE Select
|
ENSP00000490491.2:p.Ala1307=
|
|
ENST00000636940.1:n.1918T>C
|
|
|
ENST00000637015.1:c.1289T>C
|
|
|
ENST00000637568.1:c.1203T>C
|
|
|
ENST00000637741.1:n.587T>C
|
|
|
ENST00000637810.1:c.1263T>C
|
ENSP00000489636.1:p.Ala421=
|
|
ENST00000637904.1:c.1422T>C
|
ENSP00000490550.1:p.Ala474=
|
|
ENST00000647938.1:c.3552T>C
|
ENSP00000498155.1:p.Ala1184=
|
|
ENST00000346085.9:c.3552T>C
|
ENSP00000344546.4:p.Ala1184=
|
|
ENST00000350026.9:c.3513T>C
|
ENSP00000055163.7:p.Ala1171=
|
|
ENST00000414678.6:c.2079T>C
|
ENSP00000412835.2:p.Ala693=
|
|
NM_017519.2:c.3513T>C
|
NP_059989.2:p.Ala1171=
|
|
NM_020732.3:c.3552T>C
|
NP_065783.3:p.Ala1184=
|
|
XM_005267069.3:c.3672T>C
|
XP_005267126.2:p.Ala1224=
|
|
XM_011535984.1:c.2751T>C
|
XP_011534286.1:p.Ala917=
|
|
XM_011535985.1:c.2571T>C
|
XP_011534287.1:p.Ala857=
|
|
XM_011535986.1:c.2331T>C
|
XP_011534288.1:p.Ala777=
|
|
XM_011535987.1:c.1950T>C
|
XP_011534289.1:p.Ala650=
|
|
XM_011535988.1:c.813T>C
|
XP_011534290.1:p.Ala271=
|
|
NM_001346813.1:c.3672T>C
|
NP_001333742.1:p.Ala1224=
|
|
NM_001363725.1:c.1422T>C
|
NP_001350654.1:p.Ala474=
|
|
XM_011535984.2:c.3882T>C
|
XP_011534286.2:p.Ala1294=
|
|
XM_011535988.3:c.813T>C
|
XP_011534290.1:p.Ala271=
|
|
XM_017011103.2:c.3783T>C
|
XP_016866592.1:p.Ala1261=
|
|
XM_017011104.1:c.3753T>C
|
XP_016866593.1:p.Ala1251=
|
|
XM_017011105.2:c.3723T>C
|
XP_016866594.1:p.Ala1241=
|
|
XM_017011106.2:c.3594T>C
|
XP_016866595.1:p.Ala1198=
|
|
XM_017011107.2:c.3573T>C
|
XP_016866596.1:p.Ala1191=
|
|
XR_002956289.1:n.3965T>C
|
|
|
NM_001363725.2:c.1422T>C
|
NP_001350654.1:p.Ala474=
|
|
NM_001371656.1:c.3801T>C
|
NP_001358585.1:p.Ala1267=
|
|
NM_001374820.1:c.3801T>C
|
NP_001361749.1:p.Ala1267=
|
|
NM_001374828.1:c.3921T>C
MANE Select
|
NP_001361757.1:p.Ala1307=
|
|
NM_017519.3:c.3762T>C
|
NP_059989.3:p.Ala1254=
|
|