ENST00000262367.10:c.7156G>T
MANE Select
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ENSP00000262367.5:p.Gly2386Ter
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ENST00000262367.9:c.7156G>T
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ENSP00000262367.5:p.Gly2386Ter
|
|
ENST00000382070.7:c.7042G>T
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ENSP00000371502.3:p.Gly2348Ter
|
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NM_001079846.1:c.7042G>T
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NP_001073315.1:p.Gly2348Ter
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NM_004380.2:c.7156G>T
|
NP_004371.2:p.Gly2386Ter
|
|
XM_005255124.3:c.7111G>T
|
XP_005255181.1:p.Gly2371Ter
|
|
XM_005255125.3:c.6739G>T
|
XP_005255182.1:p.Gly2247Ter
|
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XM_006720848.2:c.6895G>T
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XP_006720911.1:p.Gly2299Ter
|
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XM_011522380.1:c.7102G>T
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XP_011520682.1:p.Gly2368Ter
|
|
XM_011522381.1:c.6403G>T
|
XP_011520683.1:p.Gly2135Ter
|
|
XM_005255124.4:c.7111G>T
|
XP_005255181.1:p.Gly2371Ter
|
|
XM_005255125.4:c.6739G>T
|
XP_005255182.1:p.Gly2247Ter
|
|
XM_006720848.3:c.6895G>T
|
XP_006720911.1:p.Gly2299Ter
|
|
XM_011522381.2:c.6403G>T
|
XP_011520683.1:p.Gly2135Ter
|
|
XM_017022944.1:c.7150G>T
|
XP_016878433.1:p.Gly2384Ter
|
|
NM_004380.3:c.7156G>T
MANE Select
|
NP_004371.2:p.Gly2386Ter
|
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