ENST00000685187.1:n.1442-121C>T
|
|
|
ENST00000685801.1:c.1228-121C>T
|
ENSP00000510688.1:n.1228-121C>T
|
|
ENST00000691109.1:n.1523-121C>T
|
|
|
ENST00000691687.1:n.2026-121C>T
|
|
|
ENST00000692930.1:n.1442-121C>T
|
|
|
ENST00000216181.11:c.1228-121C>T
MANE Select
|
ENSP00000216181.6:n.1228-121C>T
|
|
ENST00000216181.9:c.1228-121C>T
|
ENSP00000216181.5:n.1228-121C>T
|
|
ENST00000477189.1:n.416-121C>T
|
|
|
NM_002473.5:c.1228-121C>T , LRG_567t1:c.1228-121C>T
|
NP_002464.1:n.1228-121C>T
|
|
XM_011530197.1:c.1228-121C>T
|
XP_011528499.1:n.1228-121C>T
|
|
XM_011530197.2:c.1228-121C>T
|
XP_011528499.1:n.1228-121C>T
|
|
XM_017028803.1:c.1228-121C>T
|
XP_016884292.1:n.1228-121C>T
|
|
XM_017028804.1:c.1228-121C>T
|
XP_016884293.1:n.1228-121C>T
|
|
XM_017028805.1:c.1228-121C>T
|
XP_016884294.1:n.1228-121C>T
|
|
XM_017028806.1:c.1228-121C>T
|
XP_016884295.1:n.1228-121C>T
|
|
NM_002473.6:c.1228-121C>T
MANE Select
|
NP_002464.1:n.1228-121C>T
|
|