ENST00000587504.6:c.932+2T>C
|
ENSP00000514388.1:n.932+2T>C
|
|
ENST00000699511.1:c.131+2T>C
|
|
|
ENST00000207549.9:c.951+2T>C
MANE Select
|
ENSP00000207549.3:n.951+2T>C
|
|
ENST00000207549.8:c.951+2T>C
|
ENSP00000207549.3:n.951+2T>C
|
|
ENST00000412096.6:c.951+2T>C
|
ENSP00000388093.1:n.951+2T>C
|
|
ENST00000586147.1:c.118-3760T>C
|
ENSP00000466543.1:n.118-3760T>C
|
|
ENST00000587105.1:c.173+2T>C
|
|
|
ENST00000587504.5:n.954+2T>C
|
|
|
ENST00000591563.5:n.1148T>C
|
|
|
NM_199242.2:c.951+2T>C , LRG_122t1:c.951+2T>C
|
NP_954712.1:n.951+2T>C
|
|
XM_011524504.1:c.951+2T>C
|
XP_011522806.1:n.951+2T>C
|
|
XM_011524505.1:c.951+2T>C
|
XP_011522807.1:n.951+2T>C
|
|
XM_011524506.1:c.951+2T>C
|
XP_011522808.1:n.951+2T>C
|
|
XM_011524507.1:c.342+2T>C
|
XP_011522809.1:n.342+2T>C
|
|
XM_011524508.1:c.342+2T>C
|
XP_011522810.1:n.342+2T>C
|
|
XM_011524504.2:c.951+2T>C
|
XP_011522806.1:n.951+2T>C
|
|
XM_011524507.2:c.342+2T>C
|
XP_011522809.1:n.342+2T>C
|
|
XM_024450640.1:c.342+2T>C
|
XP_024306408.1:n.342+2T>C
|
|
NM_199242.3:c.951+2T>C
MANE Select
|
NP_954712.1:n.951+2T>C
|
|