ENST00000353383.6:c.814_815insCA
MANE Select
|
ENSP00000323074.4:p.Gly272AlafsTer?
|
|
ENST00000640861.1:c.748_749insCA
|
ENSP00000491773.1:p.Gly250AlafsTer?
|
|
ENST00000353383.5:c.814_815insCA
|
ENSP00000323074.4:p.Gly272AlafsTer?
|
|
ENST00000395774.1:c.814_815insCA
|
ENSP00000379120.1:p.Gly272AlafsTer?
|
|
NM_030665.3:c.814_815insCA
|
NP_109590.3:p.Gly272AlafsTer?
|
|
XM_017024025.1:c.814_815insCA
|
XP_016879514.1:p.Gly272AlafsTer?
|
|
XM_017024026.1:c.814_815insCA
|
XP_016879515.1:p.Gly272AlafsTer?
|
|
XM_017024027.1:c.814_815insCA
|
XP_016879516.1:p.Gly272AlafsTer?
|
|
XM_017024028.2:c.814_815insCA
|
XP_016879517.1:p.Gly272AlafsTer?
|
|
NM_030665.4:c.814_815insCA
MANE Select
|
NP_109590.3:p.Gly272AlafsTer?
|
|