ENST00000684241.1:n.3792C>G
|
|
|
ENST00000262186.10:c.2959C>G
MANE Select
|
ENSP00000262186.5:p.Leu987Val
|
|
ENST00000330883.9:c.1939C>G
|
ENSP00000328531.4:p.Leu647Val
|
|
ENST00000262186.9:c.2959C>G
|
ENSP00000262186.5:p.Leu987Val
|
|
ENST00000330883.8:c.1939C>G
|
ENSP00000328531.4:p.Leu647Val
|
|
NM_000238.3:c.2959C>G , LRG_288t1:c.2959C>G
|
NP_000229.1:p.Leu987Val
|
|
NM_172057.2:c.1939C>G , LRG_288t3:c.1939C>G
|
NP_742054.1:p.Leu647Val
|
|
XM_011516185.1:c.2659C>G
|
XP_011514487.1:p.Leu887Val
|
|
XM_011516186.1:c.*39C>G
|
XP_011514488.1:n.*39C>G
|
|
XM_011516185.2:c.2659C>G
|
XP_011514487.1:p.Leu887Val
|
|
XM_011516186.3:c.*39C>G
|
XP_011514488.1:n.*39C>G
|
|
XM_017012195.1:c.2809C>G
|
XP_016867684.1:p.Leu937Val
|
|
XM_017012196.1:c.2782C>G
|
XP_016867685.1:p.Leu928Val
|
|
NM_000238.4:c.2959C>G
MANE Select
|
NP_000229.1:p.Leu987Val
|
|
NM_172057.3:c.1939C>G
|
NP_742054.1:p.Leu647Val
|
|