ENST00000321612.8:c.1918C>G
MANE Select
|
ENSP00000370737.4:p.His640Asp
|
|
ENST00000460457.2:n.78C>G
|
|
|
ENST00000638233.1:n.353C>G
|
|
|
ENST00000638661.1:c.118C>G
|
ENSP00000491369.1:p.His40Asp
|
|
ENST00000638694.1:n.105C>G
|
|
|
ENST00000639318.1:c.118C>G
|
ENSP00000491932.1:p.His40Asp
|
|
ENST00000639364.1:n.1618C>G
|
|
|
ENST00000639443.1:n.1486C>G
|
|
|
ENST00000639954.1:n.1626C>G
|
|
|
ENST00000640208.1:c.118C>G
|
ENSP00000491895.1:p.His40Asp
|
|
ENST00000640505.1:n.157C>G
|
|
|
ENST00000640592.1:n.1801C>G
|
|
|
ENST00000321612.6:c.1918C>G
|
ENSP00000370737.3:p.His640Asp
|
|
ENST00000460457.1:n.57C>G
|
|
|
NM_000170.2:c.1918C>G , LRG_643t1:c.1918C>G
|
NP_000161.2:p.His640Asp
|
|
NM_000170.3:c.1918C>G
MANE Select
|
NP_000161.2:p.His640Asp
|
|