ENST00000649448.1:c.832A>G
|
ENSP00000497165.1:p.Met278Val
|
|
ENST00000650372.1:c.2515A>G
MANE Select
|
ENSP00000497931.1:p.Met839Val
|
|
ENST00000263817.6:c.2515A>G
|
ENSP00000263817.6:p.Met839Val
|
|
ENST00000439188.1:c.1204A>G
|
ENSP00000416058.1:n.1204A>G
|
|
NM_003742.2:c.2515A>G
|
NP_003733.2:p.Met839Val
|
|
XM_006712817.2:c.2557A>G
|
XP_006712880.1:p.Met853Val
|
|
XM_011512077.1:c.2617A>G
|
XP_011510379.1:p.Met873Val
|
|
XM_011512078.1:c.2617A>G
|
XP_011510380.1:p.Met873Val
|
|
XM_011512079.1:c.2617A>G
|
XP_011510381.1:p.Met873Val
|
|
XM_011512080.1:c.2617A>G
|
XP_011510382.1:p.Met873Val
|
|
XM_011512081.1:c.841A>G
|
XP_011510383.1:p.Met281Val
|
|
NM_003742.4:c.2515A>G
MANE Select
|
NP_003733.2:p.Met839Val
|
|
XM_006712817.3:c.2557A>G
|
XP_006712880.1:p.Met853Val
|
|
XM_011512077.2:c.2617A>G
|
XP_011510379.1:p.Met873Val
|
|
XM_011512078.2:c.2617A>G
|
XP_011510380.1:p.Met873Val
|
|
XM_011512080.2:c.2617A>G
|
XP_011510382.1:p.Met873Val
|
|
XM_011512081.2:c.841A>G
|
XP_011510383.1:p.Met281Val
|
|
XM_017005165.1:c.2617A>G
|
XP_016860654.1:p.Met873Val
|
|
XM_017005166.1:c.1846A>G
|
XP_016860655.1:p.Met616Val
|
|
XM_017005167.1:c.1300A>G
|
XP_016860656.1:p.Met434Val
|
|