ENST00000422440.7:c.293T>C
MANE Select
|
ENSP00000388658.2:p.Phe98Ser
|
|
ENST00000263812.8:c.210-11358T>C
|
ENSP00000263812.4:n.210-11358T>C
|
|
ENST00000422440.6:c.293T>C
|
ENSP00000388658.2:p.Phe98Ser
|
|
ENST00000426896.5:c.293T>C
|
ENSP00000413968.1:p.Phe98Ser
|
|
ENST00000472748.5:n.458T>C
|
|
|
ENST00000475360.6:c.281T>C
|
ENSP00000437845.1:p.Phe94Ser
|
|
ENST00000484227.5:n.491T>C
|
|
|
NM_003705.4:c.293T>C
|
NP_003696.2:p.Phe98Ser
|
|
NR_047549.1:n.302-11358T>C
|
|
|
XM_005246923.3:c.242T>C
|
XP_005246980.1:p.Phe81Ser
|
|
XM_011512069.1:c.293T>C
|
XP_011510371.1:p.Phe98Ser
|
|
XM_011512070.1:c.-85T>C
|
XP_011510372.1:n.-85T>C
|
|
XM_011512070.3:c.-85T>C
|
XP_011510372.1:n.-85T>C
|
|
NM_003705.5:c.293T>C
MANE Select
|
NP_003696.2:p.Phe98Ser
|
|
NR_047549.2:n.240-11358T>C
|
|
|