ENST00000684241.1:n.1413G=
|
|
|
ENST00000262186.10:c.580G=
MANE Select
|
ENSP00000262186.5:p.Val194=
|
|
ENST00000262186.9:c.580G=
|
ENSP00000262186.5:p.Val194=
|
|
ENST00000430723.4:c.235-3G=
|
ENSP00000387657.4:n.235-3G=
|
|
ENST00000532957.5:n.803G=
|
|
|
NM_000238.3:c.580G= , LRG_288t1:c.580G=
|
NP_000229.1:p.Val194=
|
|
NM_172056.2:c.580G= , LRG_288t2:c.580G=
|
NP_742053.1:p.Val194=
|
|
XM_011516185.1:c.280G=
|
XP_011514487.1:p.Val94=
|
|
XM_011516186.1:c.580G=
|
XP_011514488.1:p.Val194=
|
|
XM_011516185.2:c.280G=
|
XP_011514487.1:p.Val94=
|
|
XM_011516186.3:c.580G=
|
XP_011514488.1:p.Val194=
|
|
XM_017012195.1:c.430G=
|
XP_016867684.1:p.Val144=
|
|
XM_017012196.1:c.403G=
|
XP_016867685.1:p.Val135=
|
|
NM_000238.4:c.580G=
MANE Select
|
NP_000229.1:p.Val194=
|
|