ENST00000324071.10:c.1294+50T>C
MANE Select
|
ENSP00000324648.2:n.1294+50T>C
|
|
ENST00000598834.2:c.1177-108T>C
|
|
|
ENST00000324071.8:c.1294+50T>C
|
ENSP00000324648.2:n.1294+50T>C
|
|
ENST00000593831.1:c.586+50T>C
|
ENSP00000470582.1:n.586+50T>C
|
|
ENST00000597612.1:n.647+380T>C
|
|
|
NM_000767.4:c.1294+50T>C
|
NP_000758.1:n.1294+50T>C
|
|
XM_005258569.3:c.1152+380T>C
|
XP_005258626.1:n.1152+380T>C
|
|
XM_006723050.2:c.1294+50T>C
|
XP_006723113.1:n.1294+50T>C
|
|
XM_011526546.1:c.1202T>C
|
XP_011524848.1:p.Ile401Thr
|
|
XM_011526547.1:c.1153-108T>C
|
XP_011524849.1:n.1153-108T>C
|
|
XM_011526548.1:c.814+50T>C
|
XP_011524850.1:n.814+50T>C
|
|
XM_011526549.1:c.703+50T>C
|
XP_011524851.1:n.703+50T>C
|
|
XM_011526550.1:c.694+50T>C
|
XP_011524852.1:n.694+50T>C
|
|
NM_000767.5:c.1294+50T>C
MANE Select
|
NP_000758.1:n.1294+50T>C
|
|