ENST00000706527.1:n.1111+575G>T
|
|
|
ENST00000282397.9:c.3286+575G>T
MANE Select
|
ENSP00000282397.4:n.3286+575G>T
|
|
ENST00000282397.8:c.3286+575G>T
|
ENSP00000282397.4:n.3286+575G>T
|
|
ENST00000540678.2:c.-474+575G>T
|
ENSP00000443311.2:n.-474+575G>T
|
|
ENST00000543394.2:c.355+575G>T
|
ENSP00000437841.1:n.355+575G>T
|
|
ENST00000615611.4:c.571+575G>T
|
ENSP00000484385.1:n.571+575G>T
|
|
NM_002019.4:c.3286+575G>T
MANE Select
|
NP_002010.2:n.3286+575G>T
|
|
XR_941797.1:n.1237C>A
|
|
|
XR_941798.1:n.917+5068C>A
|
|
|
XM_017020485.1:c.3172+575G>T
|
XP_016875974.1:n.3172+575G>T
|
|