ENST00000647165.2:c.6473T>C
MANE Select
|
ENSP00000495481.1:p.Phe2158Ser
|
|
ENST00000205890.9:c.6473T>C
|
ENSP00000205890.5:p.Phe2158Ser
|
|
ENST00000578999.1:n.58T>C
|
|
|
ENST00000615845.4:c.6473T>C
|
ENSP00000481642.1:p.Phe2158Ser
|
|
NM_016239.3:c.6473T>C
|
NP_057323.3:p.Phe2158Ser
|
|
XM_011523917.1:c.6413T>C
|
XP_011522219.1:p.Phe2138Ser
|
|
XM_011523918.1:c.6342+71T>C
|
XP_011522220.1:n.6342+71T>C
|
|
XM_011523921.1:c.6467T>C
|
XP_011522223.1:p.Phe2156Ser
|
|
XR_934037.1:n.7072T>C
|
|
|
XR_934038.1:n.7072T>C
|
|
|
XM_011523918.2:c.6342+71T>C
|
XP_011522220.1:n.6342+71T>C
|
|
XM_017024714.2:c.6413T>C
|
XP_016880203.1:p.Phe2138Ser
|
|
XM_017024715.2:c.6476T>C
|
XP_016880204.1:p.Phe2159Ser
|
|
XM_024450781.1:c.6213+1479T>C
|
XP_024306549.1:n.6213+1479T>C
|
|
NM_016239.4:c.6473T>C
MANE Select
|
NP_057323.3:p.Phe2158Ser
|
|