ENST00000684241.1:n.1505G>C
|
|
|
ENST00000262186.10:c.672G>C
MANE Select
|
ENSP00000262186.5:p.Gly224=
|
|
ENST00000262186.9:c.672G>C
|
ENSP00000262186.5:p.Gly224=
|
|
ENST00000430723.4:c.324G>C
|
ENSP00000387657.4:p.Gly108=
|
|
ENST00000532957.5:n.895G>C
|
|
|
NM_000238.3:c.672G>C , LRG_288t1:c.672G>C
|
NP_000229.1:p.Gly224=
|
|
NM_172056.2:c.672G>C , LRG_288t2:c.672G>C
|
NP_742053.1:p.Gly224=
|
|
XM_011516185.1:c.372G>C
|
XP_011514487.1:p.Gly124=
|
|
XM_011516186.1:c.672G>C
|
XP_011514488.1:p.Gly224=
|
|
XM_011516185.2:c.372G>C
|
XP_011514487.1:p.Gly124=
|
|
XM_011516186.3:c.672G>C
|
XP_011514488.1:p.Gly224=
|
|
XM_017012195.1:c.522G>C
|
XP_016867684.1:p.Gly174=
|
|
XM_017012196.1:c.495G>C
|
XP_016867685.1:p.Gly165=
|
|
NM_000238.4:c.672G>C
MANE Select
|
NP_000229.1:p.Gly224=
|
|