ENST00000377833.10:c.10748G>C
MANE Select
|
ENSP00000367064.4:p.Gly3583Ala
|
|
ENST00000377833.8:c.10748G>C
|
ENSP00000367064.4:p.Gly3583Ala
|
|
NM_001081.3:c.10748G>C , LRG_540t1:c.10748G>C
|
NP_001072.2:p.Gly3583Ala
|
|
XM_011519709.1:c.6734G>C
|
XP_011518011.1:p.Gly2245Ala
|
|
XM_011519710.1:c.6710G>C
|
XP_011518012.1:p.Gly2237Ala
|
|
XM_011519711.1:c.6590G>C
|
XP_011518013.1:p.Gly2197Ala
|
|
XM_011519709.2:c.6734G>C
|
XP_011518011.1:p.Gly2245Ala
|
|
XM_011519710.2:c.6710G>C
|
XP_011518012.1:p.Gly2237Ala
|
|
XM_011519711.3:c.6590G>C
|
XP_011518013.1:p.Gly2197Ala
|
|
NM_001081.4:c.10748G>C
MANE Select
|
NP_001072.2:p.Gly3583Ala
|
|