ENST00000262367.10:c.7323C>G
MANE Select
|
ENSP00000262367.5:p.Gly2441=
|
|
ENST00000262367.9:c.7323C>G
|
ENSP00000262367.5:p.Gly2441=
|
|
ENST00000382070.7:c.7209C>G
|
ENSP00000371502.3:p.Gly2403=
|
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NM_001079846.1:c.7209C>G
|
NP_001073315.1:p.Gly2403=
|
|
NM_004380.2:c.7323C>G
|
NP_004371.2:p.Gly2441=
|
|
XM_005255124.3:c.7278C>G
|
XP_005255181.1:p.Gly2426=
|
|
XM_005255125.3:c.6906C>G
|
XP_005255182.1:p.Gly2302=
|
|
XM_006720848.2:c.7062C>G
|
XP_006720911.1:p.Gly2354=
|
|
XM_011522380.1:c.7269C>G
|
XP_011520682.1:p.Gly2423=
|
|
XM_011522381.1:c.6570C>G
|
XP_011520683.1:p.Gly2190=
|
|
XM_005255124.4:c.7278C>G
|
XP_005255181.1:p.Gly2426=
|
|
XM_005255125.4:c.6906C>G
|
XP_005255182.1:p.Gly2302=
|
|
XM_006720848.3:c.7062C>G
|
XP_006720911.1:p.Gly2354=
|
|
XM_011522381.2:c.6570C>G
|
XP_011520683.1:p.Gly2190=
|
|
XM_017022944.1:c.7317C>G
|
XP_016878433.1:p.Gly2439=
|
|
NM_004380.3:c.7323C>G
MANE Select
|
NP_004371.2:p.Gly2441=
|
|