ENST00000336505.11:c.1674+3141T>C
MANE Select
|
ENSP00000336756.6:n.1674+3141T>C
|
|
ENST00000336505.10:c.1674+3141T>C
|
ENSP00000336756.5:n.1674+3141T>C
|
|
ENST00000373549.8:c.1743+3141T>C
|
ENSP00000362650.4:n.1743+3141T>C
|
|
ENST00000467917.5:c.606+3141T>C
|
|
|
ENST00000477186.5:c.*119+3141T>C
|
ENSP00000419576.1:n.*119+3141T>C
|
|
NM_001144877.2:c.1674+3141T>C
|
NP_001138349.1:n.1674+3141T>C
|
|
NM_173690.4:c.1743+3141T>C
|
NP_775961.2:n.1743+3141T>C
|
|
XR_929767.1:n.1945+3141T>C
|
|
|
NM_001144877.3:c.1674+3141T>C
MANE Select
|
NP_001138349.1:n.1674+3141T>C
|
|
NM_173690.5:c.1743+3141T>C
|
NP_775961.2:n.1743+3141T>C
|
|