ENST00000324071.10:c.1294+5G>A
MANE Select
|
ENSP00000324648.2:n.1294+5G>A
|
|
ENST00000598834.2:c.1177-153G>A
|
|
|
ENST00000324071.8:c.1294+5G>A
|
ENSP00000324648.2:n.1294+5G>A
|
|
ENST00000593831.1:c.586+5G>A
|
ENSP00000470582.1:n.586+5G>A
|
|
ENST00000597612.1:n.647+335G>A
|
|
|
NM_000767.4:c.1294+5G>A
|
NP_000758.1:n.1294+5G>A
|
|
XM_005258569.3:c.1152+335G>A
|
XP_005258626.1:n.1152+335G>A
|
|
XM_006723050.2:c.1294+5G>A
|
XP_006723113.1:n.1294+5G>A
|
|
XM_011526546.1:c.1157G>A
|
XP_011524848.1:p.Ser386Asn
|
|
XM_011526547.1:c.1153-153G>A
|
XP_011524849.1:n.1153-153G>A
|
|
XM_011526548.1:c.814+5G>A
|
XP_011524850.1:n.814+5G>A
|
|
XM_011526549.1:c.703+5G>A
|
XP_011524851.1:n.703+5G>A
|
|
XM_011526550.1:c.694+5G>A
|
XP_011524852.1:n.694+5G>A
|
|
NM_000767.5:c.1294+5G>A
MANE Select
|
NP_000758.1:n.1294+5G>A
|
|