ENST00000353383.6:c.694G>C
MANE Select
|
ENSP00000323074.4:p.Gly232Arg
|
|
ENST00000640861.1:c.629G>C
|
ENSP00000491773.1:p.Gly210Ala
|
|
ENST00000353383.5:c.694G>C
|
ENSP00000323074.4:p.Gly232Arg
|
|
ENST00000395774.1:c.694G>C
|
ENSP00000379120.1:p.Gly232Arg
|
|
NM_030665.3:c.694G>C
|
NP_109590.3:p.Gly232Arg
|
|
XM_017024025.1:c.694G>C
|
XP_016879514.1:p.Gly232Arg
|
|
XM_017024026.1:c.694G>C
|
XP_016879515.1:p.Gly232Arg
|
|
XM_017024027.1:c.694G>C
|
XP_016879516.1:p.Gly232Arg
|
|
XM_017024028.2:c.694G>C
|
XP_016879517.1:p.Gly232Arg
|
|
NM_030665.4:c.694G>C
MANE Select
|
NP_109590.3:p.Gly232Arg
|
|