ENST00000647165.2:c.6464T>A
MANE Select
|
ENSP00000495481.1:p.Leu2155His
|
|
ENST00000205890.9:c.6464T>A
|
ENSP00000205890.5:p.Leu2155His
|
|
ENST00000578999.1:n.49T>A
|
|
|
ENST00000615845.4:c.6464T>A
|
ENSP00000481642.1:p.Leu2155His
|
|
NM_016239.3:c.6464T>A
|
NP_057323.3:p.Leu2155His
|
|
XM_011523917.1:c.6404T>A
|
XP_011522219.1:p.Leu2135His
|
|
XM_011523918.1:c.6342+62T>A
|
XP_011522220.1:n.6342+62T>A
|
|
XM_011523921.1:c.6458T>A
|
XP_011522223.1:p.Leu2153His
|
|
XR_934037.1:n.7063T>A
|
|
|
XR_934038.1:n.7063T>A
|
|
|
XM_011523918.2:c.6342+62T>A
|
XP_011522220.1:n.6342+62T>A
|
|
XM_017024714.2:c.6404T>A
|
XP_016880203.1:p.Leu2135His
|
|
XM_017024715.2:c.6467T>A
|
XP_016880204.1:p.Leu2156His
|
|
XM_024450781.1:c.6213+1470T>A
|
XP_024306549.1:n.6213+1470T>A
|
|
NM_016239.4:c.6464T>A
MANE Select
|
NP_057323.3:p.Leu2155His
|
|