ENST00000422440.7:c.258T>G
MANE Select
|
ENSP00000388658.2:p.Ala86=
|
|
ENST00000263812.8:c.210-11393T>G
|
ENSP00000263812.4:n.210-11393T>G
|
|
ENST00000422440.6:c.258T>G
|
ENSP00000388658.2:p.Ala86=
|
|
ENST00000426896.5:c.258T>G
|
ENSP00000413968.1:p.Ala86=
|
|
ENST00000472748.5:n.423T>G
|
|
|
ENST00000475360.6:c.246T>G
|
ENSP00000437845.1:p.Ala82=
|
|
ENST00000484227.5:n.456T>G
|
|
|
NM_003705.4:c.258T>G
|
NP_003696.2:p.Ala86=
|
|
NR_047549.1:n.302-11393T>G
|
|
|
XM_005246923.3:c.207T>G
|
XP_005246980.1:p.Ala69=
|
|
XM_011512069.1:c.258T>G
|
XP_011510371.1:p.Ala86=
|
|
XM_011512070.1:c.-120T>G
|
XP_011510372.1:n.-120T>G
|
|
XM_011512070.3:c.-120T>G
|
XP_011510372.1:n.-120T>G
|
|
NM_003705.5:c.258T>G
MANE Select
|
NP_003696.2:p.Ala86=
|
|
NR_047549.2:n.240-11393T>G
|
|
|