ENST00000422440.7:c.236C>T
MANE Select
|
ENSP00000388658.2:p.Ala79Val
|
|
ENST00000263812.8:c.210-11415C>T
|
ENSP00000263812.4:n.210-11415C>T
|
|
ENST00000422440.6:c.236C>T
|
ENSP00000388658.2:p.Ala79Val
|
|
ENST00000426896.5:c.236C>T
|
ENSP00000413968.1:p.Ala79Val
|
|
ENST00000472748.5:n.401C>T
|
|
|
ENST00000475360.6:c.224C>T
|
ENSP00000437845.1:p.Ala75Val
|
|
ENST00000484227.5:n.434C>T
|
|
|
NM_003705.4:c.236C>T
|
NP_003696.2:p.Ala79Val
|
|
NR_047549.1:n.302-11415C>T
|
|
|
XM_005246923.3:c.185C>T
|
XP_005246980.1:p.Ala62Val
|
|
XM_011512069.1:c.236C>T
|
XP_011510371.1:p.Ala79Val
|
|
XM_011512070.1:c.-142C>T
|
XP_011510372.1:n.-142C>T
|
|
XM_011512070.3:c.-142C>T
|
XP_011510372.1:n.-142C>T
|
|
NM_003705.5:c.236C>T
MANE Select
|
NP_003696.2:p.Ala79Val
|
|
NR_047549.2:n.240-11415C>T
|
|
|