ENST00000684241.1:n.3504T>G
|
|
|
ENST00000262186.10:c.2671T>G
MANE Select
|
ENSP00000262186.5:p.Phe891Val
|
|
ENST00000330883.9:c.1651T>G
|
ENSP00000328531.4:p.Phe551Val
|
|
ENST00000262186.9:c.2671T>G
|
ENSP00000262186.5:p.Phe891Val
|
|
ENST00000330883.8:c.1651T>G
|
ENSP00000328531.4:p.Phe551Val
|
|
NM_000238.3:c.2671T>G , LRG_288t1:c.2671T>G
|
NP_000229.1:p.Phe891Val
|
|
NM_172057.2:c.1651T>G , LRG_288t3:c.1651T>G
|
NP_742054.1:p.Phe551Val
|
|
XM_011516185.1:c.2371T>G
|
XP_011514487.1:p.Phe791Val
|
|
XM_011516186.1:c.2671T>G
|
XP_011514488.1:p.Phe891Val
|
|
XM_011516185.2:c.2371T>G
|
XP_011514487.1:p.Phe791Val
|
|
XM_011516186.3:c.2671T>G
|
XP_011514488.1:p.Phe891Val
|
|
XM_017012195.1:c.2521T>G
|
XP_016867684.1:p.Phe841Val
|
|
XM_017012196.1:c.2494T>G
|
XP_016867685.1:p.Phe832Val
|
|
NM_000238.4:c.2671T>G
MANE Select
|
NP_000229.1:p.Phe891Val
|
|
NM_172057.3:c.1651T>G
|
NP_742054.1:p.Phe551Val
|
|