ENST00000379375.6:c.637T>G
MANE Select
|
ENSP00000368683.5:p.Ter213Gly
|
|
ENST00000379375.5:c.637T>G
|
ENSP00000368683.5:p.Ter213Gly
|
|
NM_001168319.1:c.634T>G
|
NP_001161791.1:p.Ter212Gly
|
|
NM_001955.4:c.637T>G
|
NP_001946.3:p.Ter213Gly
|
|
XM_011514330.1:c.637T>G
|
XP_011512632.1:p.Ter213Gly
|
|
XM_011514331.1:c.637T>G
|
XP_011512633.1:p.Ter213Gly
|
|
XM_011514332.1:c.634T>G
|
XP_011512634.1:p.Ter212Gly
|
|
XM_011514330.2:c.637T>G
|
XP_011512632.1:p.Ter213Gly
|
|
XM_011514331.3:c.637T>G
|
XP_011512633.1:p.Ter213Gly
|
|
XM_011514332.2:c.634T>G
|
XP_011512634.1:p.Ter212Gly
|
|
XM_017010331.1:c.637T>G
|
XP_016865820.1:p.Ter213Gly
|
|
NM_001955.5:c.637T>G
MANE Select
|
NP_001946.3:p.Ter213Gly
|
|
NM_001168319.2:c.634T>G
|
NP_001161791.1:p.Ter212Gly
|
|