ENST00000360256.9:c.6900+18G>T
MANE Select
|
ENSP00000353393.4:n.6900+18G>T
|
|
ENST00000644698.1:c.633+18G>T
|
ENSP00000495706.1:n.633+18G>T
|
|
ENST00000330287.10:c.495+18G>T
|
ENSP00000327895.6:n.495+18G>T
|
|
ENST00000360256.8:c.6900+18G>T
|
ENSP00000353393.4:n.6900+18G>T
|
|
NM_000132.3:c.6900+18G>T
|
NP_000123.1:n.6900+18G>T
|
|
NM_019863.2:c.495+18G>T
|
NP_063916.1:n.495+18G>T
|
|
XM_011531126.1:c.6795+18G>T
|
XP_011529428.1:n.6795+18G>T
|
|
NM_000132.4:c.6900+18G>T
MANE Select
|
NP_000123.1:n.6900+18G>T
|
|
NM_019863.3:c.495+18G>T
|
NP_063916.1:n.495+18G>T
|
|