ENST00000394867.9:n.1572A>G
|
|
|
ENST00000688002.1:n.3284A>G
|
|
|
ENST00000688751.1:n.269A>G
|
|
|
ENST00000689792.1:n.1037A>G
|
|
|
ENST00000262948.10:c.1133A>G
MANE Select
|
ENSP00000262948.4:p.Asp378Gly
|
|
ENST00000262948.9:c.1133A>G
|
ENSP00000262948.3:p.Asp378Gly
|
|
ENST00000394867.8:c.842A>G
|
ENSP00000378336.1:p.Asp281Gly
|
|
ENST00000597263.5:n.318A>G
|
|
|
ENST00000599021.1:c.243A>G
|
|
|
ENST00000600584.5:n.2582A>G
|
|
|
ENST00000601786.5:n.1434A>G
|
|
|
NM_030662.3:c.1133A>G , LRG_750t1:c.1133A>G
|
NP_109587.1:p.Asp378Gly
|
|
XM_006722799.2:c.854A>G
|
XP_006722862.1:p.Asp285Gly
|
|
XM_011528133.1:c.563A>G
|
XP_011526435.1:p.Asp188Gly
|
|
NM_030662.4:c.1133A>G
MANE Select
|
NP_109587.1:p.Asp378Gly
|
|