ENST00000262367.10:c.4084G=
MANE Select
|
ENSP00000262367.5:p.Val1362=
|
|
ENST00000262367.9:c.4084G=
|
ENSP00000262367.5:p.Val1362=
|
|
ENST00000382070.7:c.3970G=
|
ENSP00000371502.3:p.Val1324=
|
|
ENST00000570939.2:c.2719G=
|
ENSP00000461002.2:p.Val907=
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ENST00000572569.1:n.548G=
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|
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ENST00000573517.6:c.390G=
|
|
|
ENST00000574740.1:n.166G=
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|
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ENST00000576720.1:n.3021G=
|
|
|
NM_001079846.1:c.3970G=
|
NP_001073315.1:p.Val1324=
|
|
NM_004380.2:c.4084G=
|
NP_004371.2:p.Val1362=
|
|
XM_005255124.3:c.4039G=
|
XP_005255181.1:p.Val1347=
|
|
XM_005255125.3:c.3667G=
|
XP_005255182.1:p.Val1223=
|
|
XM_006720848.2:c.4084G=
|
XP_006720911.1:p.Val1362=
|
|
XM_011522380.1:c.4030G=
|
XP_011520682.1:p.Val1344=
|
|
XM_011522381.1:c.3331G=
|
XP_011520683.1:p.Val1111=
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|
XM_005255124.4:c.4039G=
|
XP_005255181.1:p.Val1347=
|
|
XM_005255125.4:c.3667G=
|
XP_005255182.1:p.Val1223=
|
|
XM_006720848.3:c.4084G=
|
XP_006720911.1:p.Val1362=
|
|
XM_011522381.2:c.3331G=
|
XP_011520683.1:p.Val1111=
|
|
XM_017022944.1:c.4078G=
|
XP_016878433.1:p.Val1360=
|
|
NM_004380.3:c.4084G=
MANE Select
|
NP_004371.2:p.Val1362=
|
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