ENST00000636168.2:c.29G>C
|
ENSP00000490338.2:p.Gly10Ala
|
|
ENST00000672640.1:c.29G>C
|
ENSP00000500507.1:p.Gly10Ala
|
|
ENST00000261007.9:c.593G>C
|
ENSP00000261007.5:p.Gly198Ala
|
|
ENST00000348749.9:c.518G>C
MANE Select
|
ENSP00000261008.5:p.Gly173Ala
|
|
ENST00000409219.5:c.518G>C
|
ENSP00000386611.1:p.Gly173Ala
|
|
ENST00000409323.1:c.518G>C
|
ENSP00000386684.1:p.Gly173Ala
|
|
ENST00000409542.5:c.272G>C
|
ENSP00000387026.1:p.Gly91Ala
|
|
ENST00000435083.5:c.*162G>C
|
ENSP00000395805.1:n.*162G>C
|
|
NM_000079.3:c.518G>C
|
NP_000070.1:p.Gly173Ala
|
|
NM_001039523.2:c.593G>C
|
NP_001034612.1:p.Gly198Ala
|
|
XM_017003256.1:c.614G>C
|
XP_016858745.1:p.Gly205Ala
|
|
XM_017003257.1:c.539G>C
|
XP_016858746.1:p.Gly180Ala
|
|
NM_000079.4:c.518G>C
MANE Select
|
NP_000070.1:p.Gly173Ala
|
|
NM_001039523.3:c.593G>C
|
NP_001034612.1:p.Gly198Ala
|
|