ENST00000684241.1:n.1468T>G
|
|
|
ENST00000262186.10:c.635T>G
MANE Select
|
ENSP00000262186.5:p.Leu212Arg
|
|
ENST00000262186.9:c.635T>G
|
ENSP00000262186.5:p.Leu212Arg
|
|
ENST00000430723.4:c.287T>G
|
ENSP00000387657.4:p.Leu96Arg
|
|
ENST00000532957.5:n.858T>G
|
|
|
NM_000238.3:c.635T>G , LRG_288t1:c.635T>G
|
NP_000229.1:p.Leu212Arg
|
|
NM_172056.2:c.635T>G , LRG_288t2:c.635T>G
|
NP_742053.1:p.Leu212Arg
|
|
XM_011516185.1:c.335T>G
|
XP_011514487.1:p.Leu112Arg
|
|
XM_011516186.1:c.635T>G
|
XP_011514488.1:p.Leu212Arg
|
|
XM_011516185.2:c.335T>G
|
XP_011514487.1:p.Leu112Arg
|
|
XM_011516186.3:c.635T>G
|
XP_011514488.1:p.Leu212Arg
|
|
XM_017012195.1:c.485T>G
|
XP_016867684.1:p.Leu162Arg
|
|
XM_017012196.1:c.458T>G
|
XP_016867685.1:p.Leu153Arg
|
|
NM_000238.4:c.635T>G
MANE Select
|
NP_000229.1:p.Leu212Arg
|
|