ENST00000371084.8:c.1262G>C
MANE Select
|
ENSP00000360125.3:p.Gly421Ala
|
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ENST00000650546.1:c.1262G>C
|
ENSP00000497812.1:p.Gly421Ala
|
|
ENST00000371083.4:c.1316G>C
|
ENSP00000360124.4:p.Gly439Ala
|
|
ENST00000371084.7:c.1262G>C
|
ENSP00000360125.3:p.Gly421Ala
|
|
ENST00000540265.5:c.671G>C
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ENSP00000443449.1:p.Gly224Ala
|
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NM_001172818.1:c.1316G>C
|
NP_001166289.1:p.Gly439Ala
|
|
NM_001172819.1:c.671G>C
|
NP_001166290.1:p.Gly224Ala
|
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NM_002633.2:c.1262G>C
|
NP_002624.2:p.Gly421Ala
|
|
NM_002633.3:c.1262G>C
MANE Select
|
NP_002624.2:p.Gly421Ala
|
|
NM_001172819.2:c.671G>C
|
NP_001166290.1:p.Gly224Ala
|
|