|
NM_001372.4:c.1901+1G>A
MANE Select
|
NP_001363.2:n.1901+1G>A
|
|
ENST00000262442.9:c.1901+1G>A
MANE Select
|
ENSP00000262442.3:n.1901+1G>A
|
|
NM_001372.3:c.1901+1G>A
|
NP_001363.2:n.1901+1G>A
|
|
ENST00000262442.8:c.1901+1G>A
|
ENSP00000262442.3:n.1901+1G>A
|
|
ENST00000454412.6:c.1901+1G>A
|
ENSP00000414874.2:n.1901+1G>A
|
|
XM_011523703.1:c.1901+1G>A
|
XP_011522005.1:n.1901+1G>A
|
|
XM_011523703.2:c.1901+1G>A
|
XP_011522005.1:n.1901+1G>A
|
|
XM_017024292.2:c.1784+1G>A
|
XP_016879781.1:n.1784+1G>A
|
|
XM_017024293.1:c.-22+1G>A
|
XP_016879782.1:n.-22+1G>A
|
|
XM_017024294.2:c.1901+1G>A
|
XP_016879783.1:n.1901+1G>A
|
|
XM_017024295.2:c.1901+1G>A
|
XP_016879784.1:n.1901+1G>A
|