ENST00000370328.4:c.342+41G>T
MANE Select
|
ENSP00000359353.3:n.342+41G>T
|
|
ENST00000370328.3:c.342+41G>T
|
ENSP00000359353.3:n.342+41G>T
|
|
ENST00000441219.5:c.*388+41G>T
|
ENSP00000389384.1:n.*388+41G>T
|
|
ENST00000465405.1:n.477G>T
|
|
|
ENST00000474932.1:n.68+41G>T
|
|
|
NM_004961.3:c.342+41G>T
|
NP_004952.2:n.342+41G>T
|
|
XM_006724813.2:c.342+41G>T
|
XP_006724876.2:n.342+41G>T
|
|
XM_011531135.1:c.3+41G>T
|
XP_011529437.1:n.3+41G>T
|
|
XM_011531136.1:c.3+41G>T
|
XP_011529438.1:n.3+41G>T
|
|
XM_011531137.1:c.342+41G>T
|
XP_011529439.1:n.342+41G>T
|
|
XM_011531138.1:c.342+41G>T
|
XP_011529440.1:n.342+41G>T
|
|
XM_011531139.1:c.342+41G>T
|
XP_011529441.1:n.342+41G>T
|
|
XM_017029387.2:c.3+41G>T
|
XP_016884876.1:n.3+41G>T
|
|
XM_017029389.2:c.3+41G>T
|
XP_016884878.1:n.3+41G>T
|
|
XM_024452360.1:c.3+41G>T
|
XP_024308128.1:n.3+41G>T
|
|
NM_004961.4:c.342+41G>T
MANE Select
|
NP_004952.2:n.342+41G>T
|
|