ENST00000371746.9:c.879A>C
|
ENSP00000360811.3:p.Gly293=
|
|
ENST00000371748.10:c.864A>C
MANE Select
|
ENSP00000360813.4:p.Gly288=
|
|
ENST00000645419.1:n.1689A>C
|
|
|
ENST00000371746.7:c.879A>C
|
ENSP00000360811.3:p.Gly293=
|
|
ENST00000371748.9:c.864A>C
|
ENSP00000360813.4:p.Gly288=
|
|
ENST00000619587.1:c.831A>C
|
ENSP00000483080.1:p.Gly277=
|
|
NM_014564.3:c.879A>C
|
NP_055379.1:p.Gly293=
|
|
NM_178138.4:c.864A>C
|
NP_835258.1:p.Gly288=
|
|
XM_005263410.1:c.831A>C
|
XP_005263467.1:p.Gly277=
|
|
NM_001363746.1:c.831A>C
|
NP_001350675.1:p.Gly277=
|
|
NM_014564.4:c.879A>C
|
NP_055379.1:p.Gly293=
|
|
NM_178138.5:c.864A>C
|
NP_835258.1:p.Gly288=
|
|
XM_017015168.1:c.792A>C
|
XP_016870657.1:p.Gly264=
|
|
NM_178138.6:c.864A>C
MANE Select
|
NP_835258.1:p.Gly288=
|
|
NM_014564.5:c.879A>C
|
NP_055379.1:p.Gly293=
|
|