ENST00000402696.9:c.1767T>C
MANE Select
|
ENSP00000385834.3:p.Pro589=
|
|
ENST00000402696.7:c.1767T>C
|
ENSP00000385834.3:p.Pro589=
|
|
ENST00000461695.1:c.498T>C
|
|
|
ENST00000467842.1:n.2761T>C
|
|
|
NM_001063.3:c.1767T>C
|
NP_001054.1:p.Pro589=
|
|
XM_011513100.1:c.1767T>C
|
XP_011511402.1:p.Pro589=
|
|
NM_001354703.1:c.1635T>C
|
NP_001341632.1:p.Pro545=
|
|
NM_001354704.1:c.1386T>C
|
NP_001341633.1:p.Pro462=
|
|
NM_001063.4:c.1767T>C
MANE Select
|
NP_001054.2:p.Pro589=
|
|
NM_001354703.2:c.1635T>C
|
NP_001341632.2:p.Pro545=
|
|
NM_001354704.2:c.1386T>C
|
NP_001341633.2:p.Pro462=
|
|