ENST00000647165.2:c.6499T>C
MANE Select
|
ENSP00000495481.1:p.Tyr2167His
|
|
ENST00000205890.9:c.6499T>C
|
ENSP00000205890.5:p.Tyr2167His
|
|
ENST00000578999.1:n.84T>C
|
|
|
ENST00000615845.4:c.6499T>C
|
ENSP00000481642.1:p.Tyr2167His
|
|
NM_016239.3:c.6499T>C
|
NP_057323.3:p.Tyr2167His
|
|
XM_011523917.1:c.6439T>C
|
XP_011522219.1:p.Tyr2147His
|
|
XM_011523918.1:c.6342+97T>C
|
XP_011522220.1:n.6342+97T>C
|
|
XM_011523921.1:c.6493T>C
|
XP_011522223.1:p.Tyr2165His
|
|
XR_934037.1:n.7098T>C
|
|
|
XR_934038.1:n.7098T>C
|
|
|
XM_011523918.2:c.6342+97T>C
|
XP_011522220.1:n.6342+97T>C
|
|
XM_017024714.2:c.6439T>C
|
XP_016880203.1:p.Tyr2147His
|
|
XM_017024715.2:c.6502T>C
|
XP_016880204.1:p.Tyr2168His
|
|
XM_024450781.1:c.6213+1505T>C
|
XP_024306549.1:n.6213+1505T>C
|
|
NM_016239.4:c.6499T>C
MANE Select
|
NP_057323.3:p.Tyr2167His
|
|