ENST00000684241.1:n.1942T>C
|
|
|
ENST00000262186.10:c.1109T>C
MANE Select
|
ENSP00000262186.5:p.Val370Ala
|
|
ENST00000262186.9:c.1109T>C
|
ENSP00000262186.5:p.Val370Ala
|
|
ENST00000430723.4:c.761T>C
|
ENSP00000387657.4:p.Val254Ala
|
|
ENST00000532957.5:n.1332T>C
|
|
|
NM_000238.3:c.1109T>C , LRG_288t1:c.1109T>C
|
NP_000229.1:p.Val370Ala
|
|
NM_172056.2:c.1109T>C , LRG_288t2:c.1109T>C
|
NP_742053.1:p.Val370Ala
|
|
XM_011516185.1:c.809T>C
|
XP_011514487.1:p.Val270Ala
|
|
XM_011516186.1:c.1109T>C
|
XP_011514488.1:p.Val370Ala
|
|
XM_011516185.2:c.809T>C
|
XP_011514487.1:p.Val270Ala
|
|
XM_011516186.3:c.1109T>C
|
XP_011514488.1:p.Val370Ala
|
|
XM_017012195.1:c.959T>C
|
XP_016867684.1:p.Val320Ala
|
|
XM_017012196.1:c.932T>C
|
XP_016867685.1:p.Val311Ala
|
|
NM_000238.4:c.1109T>C
MANE Select
|
NP_000229.1:p.Val370Ala
|
|