ENST00000541682.7:c.494A>G
MANE Select
|
ENSP00000446205.2:p.Gln165Arg
|
|
ENST00000317814.8:c.479A>G
|
ENSP00000314774.4:p.Gln160Arg
|
|
ENST00000541682.6:c.494A>G
|
ENSP00000446205.2:p.Gln165Arg
|
|
NM_001165967.1:c.494A>G
|
NP_001159439.1:p.Gln165Arg
|
|
NM_032580.3:c.479A>G
|
NP_115969.2:p.Gln160Arg
|
|
XM_011524038.1:c.599A>G
|
XP_011522340.1:p.Gln200Arg
|
|
XM_011524039.1:c.590A>G
|
XP_011522341.1:p.Gln197Arg
|
|
XM_011524040.1:c.590A>G
|
XP_011522342.1:p.Gln197Arg
|
|
XM_011524041.1:c.581A>G
|
XP_011522343.1:p.Gln194Arg
|
|
XM_011524042.1:c.452A>G
|
XP_011522344.1:p.Gln151Arg
|
|
XR_934203.1:n.69+1956T>C
|
|
|
XM_017025232.1:c.599A>G
|
XP_016880721.1:p.Gln200Arg
|
|
XM_024451007.1:c.599A>G
|
XP_024306775.1:p.Gln200Arg
|
|
NM_001165967.2:c.494A>G
MANE Select
|
NP_001159439.1:p.Gln165Arg
|
|
NM_032580.4:c.479A>G
|
NP_115969.2:p.Gln160Arg
|
|