ENST00000684241.1:n.1854G>A
|
|
|
ENST00000262186.10:c.1021G>A
MANE Select
|
ENSP00000262186.5:p.Val341Met
|
|
ENST00000262186.9:c.1021G>A
|
ENSP00000262186.5:p.Val341Met
|
|
ENST00000430723.4:c.673G>A
|
ENSP00000387657.4:p.Val225Met
|
|
ENST00000532957.5:n.1244G>A
|
|
|
NM_000238.3:c.1021G>A , LRG_288t1:c.1021G>A
|
NP_000229.1:p.Val341Met
|
|
NM_172056.2:c.1021G>A , LRG_288t2:c.1021G>A
|
NP_742053.1:p.Val341Met
|
|
XM_011516185.1:c.721G>A
|
XP_011514487.1:p.Val241Met
|
|
XM_011516186.1:c.1021G>A
|
XP_011514488.1:p.Val341Met
|
|
XM_011516185.2:c.721G>A
|
XP_011514487.1:p.Val241Met
|
|
XM_011516186.3:c.1021G>A
|
XP_011514488.1:p.Val341Met
|
|
XM_017012195.1:c.871G>A
|
XP_016867684.1:p.Val291Met
|
|
XM_017012196.1:c.844G>A
|
XP_016867685.1:p.Val282Met
|
|
NM_000238.4:c.1021G>A
MANE Select
|
NP_000229.1:p.Val341Met
|
|