ENST00000699510.1:c.337G>C
|
ENSP00000514405.1:p.Glu113Gln
|
|
ENST00000699511.1:c.579G>C
|
|
|
ENST00000207549.9:c.1402G>C
MANE Select
|
ENSP00000207549.3:p.Glu468Gln
|
|
ENST00000207549.8:c.1402G>C
|
ENSP00000207549.3:p.Glu468Gln
|
|
ENST00000412096.6:c.1402G>C
|
ENSP00000388093.1:p.Glu468Gln
|
|
ENST00000586147.1:c.130G>C
|
ENSP00000466543.1:p.Glu44Gln
|
|
ENST00000587105.1:c.521G>C
|
|
|
ENST00000591563.5:n.1672G>C
|
|
|
NM_199242.2:c.1402G>C , LRG_122t1:c.1402G>C
|
NP_954712.1:p.Glu468Gln
|
|
XM_011524504.1:c.1402G>C
|
XP_011522806.1:p.Glu468Gln
|
|
XM_011524505.1:c.1402G>C
|
XP_011522807.1:p.Glu468Gln
|
|
XM_011524506.1:c.1399G>C
|
XP_011522808.1:p.Glu467Gln
|
|
XM_011524507.1:c.793G>C
|
XP_011522809.1:p.Glu265Gln
|
|
XM_011524508.1:c.793G>C
|
XP_011522810.1:p.Glu265Gln
|
|
XM_011524504.2:c.1402G>C
|
XP_011522806.1:p.Glu468Gln
|
|
XM_011524507.2:c.793G>C
|
XP_011522809.1:p.Glu265Gln
|
|
XM_024450640.1:c.793G>C
|
XP_024306408.1:p.Glu265Gln
|
|
NM_199242.3:c.1402G>C
MANE Select
|
NP_954712.1:p.Glu468Gln
|
|