ENST00000647165.2:c.6499T>G
MANE Select
|
ENSP00000495481.1:p.Tyr2167Asp
|
|
ENST00000205890.9:c.6499T>G
|
ENSP00000205890.5:p.Tyr2167Asp
|
|
ENST00000578999.1:n.84T>G
|
|
|
ENST00000615845.4:c.6499T>G
|
ENSP00000481642.1:p.Tyr2167Asp
|
|
NM_016239.3:c.6499T>G
|
NP_057323.3:p.Tyr2167Asp
|
|
XM_011523917.1:c.6439T>G
|
XP_011522219.1:p.Tyr2147Asp
|
|
XM_011523918.1:c.6342+97T>G
|
XP_011522220.1:n.6342+97T>G
|
|
XM_011523921.1:c.6493T>G
|
XP_011522223.1:p.Tyr2165Asp
|
|
XR_934037.1:n.7098T>G
|
|
|
XR_934038.1:n.7098T>G
|
|
|
XM_011523918.2:c.6342+97T>G
|
XP_011522220.1:n.6342+97T>G
|
|
XM_017024714.2:c.6439T>G
|
XP_016880203.1:p.Tyr2147Asp
|
|
XM_017024715.2:c.6502T>G
|
XP_016880204.1:p.Tyr2168Asp
|
|
XM_024450781.1:c.6213+1505T>G
|
XP_024306549.1:n.6213+1505T>G
|
|
NM_016239.4:c.6499T>G
MANE Select
|
NP_057323.3:p.Tyr2167Asp
|
|