ENST00000262367.10:c.4210G>A
MANE Select
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ENSP00000262367.5:p.Gly1404Ser
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ENST00000262367.9:c.4210G>A
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ENSP00000262367.5:p.Gly1404Ser
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ENST00000382070.7:c.4096G>A
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ENSP00000371502.3:p.Gly1366Ser
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ENST00000570939.2:c.2845G>A
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ENSP00000461002.2:p.Gly949Ser
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ENST00000573517.6:c.516G>A
|
|
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ENST00000574740.1:n.215+751G>A
|
|
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ENST00000576720.1:n.3147G>A
|
|
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NM_001079846.1:c.4096G>A
|
NP_001073315.1:p.Gly1366Ser
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NM_004380.2:c.4210G>A
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NP_004371.2:p.Gly1404Ser
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XM_005255124.3:c.4165G>A
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XP_005255181.1:p.Gly1389Ser
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XM_005255125.3:c.3793G>A
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XP_005255182.1:p.Gly1265Ser
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XM_006720848.2:c.4133+751G>A
|
XP_006720911.1:n.4133+751G>A
|
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XM_011522380.1:c.4156G>A
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XP_011520682.1:p.Gly1386Ser
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XM_011522381.1:c.3457G>A
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XP_011520683.1:p.Gly1153Ser
|
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XM_005255124.4:c.4165G>A
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XP_005255181.1:p.Gly1389Ser
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XM_005255125.4:c.3793G>A
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XP_005255182.1:p.Gly1265Ser
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XM_006720848.3:c.4133+751G>A
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XP_006720911.1:n.4133+751G>A
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XM_011522381.2:c.3457G>A
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XP_011520683.1:p.Gly1153Ser
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XM_017022944.1:c.4204G>A
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XP_016878433.1:p.Gly1402Ser
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NM_004380.3:c.4210G>A
MANE Select
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NP_004371.2:p.Gly1404Ser
|
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