ENST00000461280.2:n.958A>G
|
|
|
ENST00000684116.1:n.553A>G
|
|
|
ENST00000684241.1:n.2493A>G
|
|
|
ENST00000262186.10:c.1660A>G
MANE Select
|
ENSP00000262186.5:p.Met554Val
|
|
ENST00000330883.9:c.640A>G
|
ENSP00000328531.4:p.Met214Val
|
|
ENST00000262186.9:c.1660A>G
|
ENSP00000262186.5:p.Met554Val
|
|
ENST00000330883.8:c.640A>G
|
ENSP00000328531.4:p.Met214Val
|
|
ENST00000430723.4:c.1312A>G
|
ENSP00000387657.4:p.Met438Val
|
|
ENST00000461280.1:n.947A>G
|
|
|
ENST00000473610.5:n.965A>G
|
|
|
ENST00000532957.5:n.1883A>G
|
|
|
NM_000238.3:c.1660A>G , LRG_288t1:c.1660A>G
|
NP_000229.1:p.Met554Val
|
|
NM_001204798.1:c.640A>G
|
NP_001191727.1:p.Met214Val
|
|
NM_172056.2:c.1660A>G , LRG_288t2:c.1660A>G
|
NP_742053.1:p.Met554Val
|
|
NM_172057.2:c.640A>G , LRG_288t3:c.640A>G
|
NP_742054.1:p.Met214Val
|
|
XM_011516185.1:c.1360A>G
|
XP_011514487.1:p.Met454Val
|
|
XM_011516186.1:c.1660A>G
|
XP_011514488.1:p.Met554Val
|
|
XM_011516185.2:c.1360A>G
|
XP_011514487.1:p.Met454Val
|
|
XM_011516186.3:c.1660A>G
|
XP_011514488.1:p.Met554Val
|
|
XM_017012195.1:c.1510A>G
|
XP_016867684.1:p.Met504Val
|
|
XM_017012196.1:c.1483A>G
|
XP_016867685.1:p.Met495Val
|
|
NM_000238.4:c.1660A>G
MANE Select
|
NP_000229.1:p.Met554Val
|
|
NM_001204798.2:c.640A>G
|
NP_001191727.1:p.Met214Val
|
|
NM_172057.3:c.640A>G
|
NP_742054.1:p.Met214Val
|
|