ENST00000644269.2:c.1457G>T
MANE Select
|
ENSP00000494017.1:p.Cys486Phe
|
|
ENST00000644846.1:c.168G>T
|
|
|
ENST00000265715.7:c.1457G>T
|
ENSP00000265715.3:p.Cys486Phe
|
|
ENST00000460748.1:n.560G>T
|
|
|
ENST00000477350.5:n.304G>T
|
|
|
ENST00000480841.5:n.306G>T
|
|
|
ENST00000497446.5:n.472G>T
|
|
|
NM_000441.1:c.1457G>T
|
NP_000432.1:p.Cys486Phe
|
|
XM_005250425.1:c.1457G>T
|
XP_005250482.1:p.Cys486Phe
|
|
XM_005250425.2:c.1457G>T
|
XP_005250482.1:p.Cys486Phe
|
|
XM_017012318.1:c.1379G>T
|
XP_016867807.1:p.Cys460Phe
|
|
NM_000441.2:c.1457G>T
MANE Select
|
NP_000432.1:p.Cys486Phe
|
|