ENST00000298910.12:c.3496G=
MANE Select
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ENSP00000298910.7:p.Ala1166=
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ENST00000679360.1:c.*2405G=
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ENSP00000505368.1:n.*2405G=
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ENST00000680790.1:c.3241G=
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ENSP00000505335.1:p.Ala1081=
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ENST00000298910.11:c.3496G=
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ENSP00000298910.7:p.Ala1166=
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ENST00000343742.6:c.3496G=
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ENSP00000341930.2:p.Ala1166=
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|
ENST00000430804.5:c.540G=
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|
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ENST00000479187.5:n.177G=
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|
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NM_198578.3:c.3496G=
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NP_940980.3:p.Ala1166=
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|
XM_005268629.2:c.3496G=
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XP_005268686.1:p.Ala1166=
|
|
XM_011537877.1:c.3496G=
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XP_011536179.1:p.Ala1166=
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|
XM_011537878.1:c.3496G=
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XP_011536180.1:p.Ala1166=
|
|
XM_011537879.1:c.2293G=
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XP_011536181.1:p.Ala765=
|
|
XM_011537880.1:c.3496G=
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XP_011536182.1:p.Ala1166=
|
|
XM_011537881.1:c.3496G=
|
XP_011536183.1:p.Ala1166=
|
|
XM_011537882.1:c.3496G=
|
XP_011536184.1:p.Ala1166=
|
|
XM_005268629.4:c.3496G=
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XP_005268686.1:p.Ala1166=
|
|
XM_011537877.3:c.3496G=
|
XP_011536179.1:p.Ala1166=
|
|
XM_011537881.3:c.3496G=
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XP_011536183.1:p.Ala1166=
|
|
XM_011537882.3:c.3496G=
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XP_011536184.1:p.Ala1166=
|
|
XM_017018786.2:c.3496G=
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XP_016874275.1:p.Ala1166=
|
|
XM_017018787.1:c.412G=
|
XP_016874276.1:p.Ala138=
|
|
XM_017018789.2:c.3496G=
|
XP_016874278.1:p.Ala1166=
|
|
XM_024448833.1:c.2293G=
|
XP_024304601.1:p.Ala765=
|
|
XR_001748574.2:n.3738G=
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NM_198578.4:c.3496G=
MANE Select
|
NP_940980.4:p.Ala1166=
|
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