ENST00000496887.7:c.1409G>C
|
ENSP00000434560.2:p.Gly470Ala
|
|
ENST00000646564.2:c.1226G>C
|
ENSP00000495806.2:p.Gly409Ala
|
|
ENST00000155840.12:c.1766G>C
MANE Select
|
ENSP00000155840.2:p.Gly589Ala
|
|
ENST00000335475.6:c.1385G>C
|
ENSP00000334497.5:p.Gly462Ala
|
|
ENST00000526095.2:c.170G>C
|
ENSP00000494939.1:p.Gly57Ala
|
|
ENST00000646564.1:c.872G>C
|
ENSP00000495806.1:p.Gly291Ala
|
|
ENST00000155840.9:c.1766G>C
|
ENSP00000155840.2:p.Gly589Ala
|
|
ENST00000335475.5:c.1385G>C
|
ENSP00000334497.5:p.Gly462Ala
|
|
ENST00000526095.1:n.273G>C
|
|
|
NM_000218.2:c.1766G>C , LRG_287t1:c.1766G>C
|
NP_000209.2:p.Gly589Ala
|
|
NM_181798.1:c.1385G>C , LRG_287t2:c.1385G>C
|
NP_861463.1:p.Gly462Ala
|
|
NM_000218.3:c.1766G>C
MANE Select
|
NP_000209.2:p.Gly589Ala
|
|