ENST00000267163.6:c.2663+150T>A
MANE Select
|
ENSP00000267163.4:n.2663+150T>A
|
|
ENST00000643064.1:c.194+95550T>A
|
|
|
ENST00000650461.1:c.2663+150T>A
|
ENSP00000497193.1:n.2663+150T>A
|
|
ENST00000267163.4:c.2663+150T>A
|
ENSP00000267163.4:n.2663+150T>A
|
|
ENST00000484879.1:n.397+150T>A
|
|
|
ENST00000531171.5:n.266+150T>A
|
|
|
NM_000321.2:c.2663+150T>A , LRG_517t1:c.2663+150T>A
|
NP_000312.2:n.2663+150T>A
|
|
XM_011535171.1:c.2402+150T>A
|
XP_011533473.1:n.2402+150T>A
|
|
XM_011535171.2:c.2402+150T>A
|
XP_011533473.1:n.2402+150T>A
|
|
NM_000321.3:c.2663+150T>A
MANE Select
|
NP_000312.2:n.2663+150T>A
|
|