ENST00000262367.10:c.1313A>G
MANE Select
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ENSP00000262367.5:p.Asp438Gly
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ENST00000262367.9:c.1313A>G
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ENSP00000262367.5:p.Asp438Gly
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|
ENST00000382070.7:c.1216+1388A>G
|
ENSP00000371502.3:n.1216+1388A>G
|
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NM_001079846.1:c.1216+1388A>G
|
NP_001073315.1:n.1216+1388A>G
|
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NM_004380.2:c.1313A>G
|
NP_004371.2:p.Asp438Gly
|
|
XM_005255124.3:c.1313A>G
|
XP_005255181.1:p.Asp438Gly
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|
XM_005255125.3:c.1313A>G
|
XP_005255182.1:p.Asp438Gly
|
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XM_006720848.2:c.1313A>G
|
XP_006720911.1:p.Asp438Gly
|
|
XM_011522380.1:c.1259A>G
|
XP_011520682.1:p.Asp420Gly
|
|
XM_011522381.1:c.560A>G
|
XP_011520683.1:p.Asp187Gly
|
|
XM_011522382.1:c.1313A>G
|
XP_011520684.1:p.Asp438Gly
|
|
XM_005255124.4:c.1313A>G
|
XP_005255181.1:p.Asp438Gly
|
|
XM_005255125.4:c.1313A>G
|
XP_005255182.1:p.Asp438Gly
|
|
XM_006720848.3:c.1313A>G
|
XP_006720911.1:p.Asp438Gly
|
|
XM_011522381.2:c.560A>G
|
XP_011520683.1:p.Asp187Gly
|
|
XM_011522382.3:c.1313A>G
|
XP_011520684.1:p.Asp438Gly
|
|
XM_017022944.1:c.1313A>G
|
XP_016878433.1:p.Asp438Gly
|
|
NM_004380.3:c.1313A>G
MANE Select
|
NP_004371.2:p.Asp438Gly
|
|