ENST00000361256.10:c.712+16C>T
MANE Select
|
ENSP00000354812.5:n.712+16C>T
|
|
ENST00000651925.1:c.*1751+16C>T
|
ENSP00000498386.1:n.*1751+16C>T
|
|
ENST00000361256.9:c.712+16C>T
|
ENSP00000354812.5:n.712+16C>T
|
|
ENST00000480366.1:n.275+16C>T
|
|
|
ENST00000622809.1:c.709+16C>T
|
ENSP00000481659.1:n.709+16C>T
|
|
NM_016390.3:c.712+16C>T
|
NP_057474.2:n.712+16C>T
|
|
XM_005252045.3:c.712+16C>T
|
XP_005252102.2:n.712+16C>T
|
|
XM_011518773.1:c.712+16C>T
|
XP_011517075.1:n.712+16C>T
|
|
XM_011518774.1:c.712+16C>T
|
XP_011517076.1:n.712+16C>T
|
|
XM_011518775.1:c.712+16C>T
|
XP_011517077.1:n.712+16C>T
|
|
XM_017014804.1:c.958+16C>T
|
XP_016870293.1:n.958+16C>T
|
|
NM_016390.4:c.712+16C>T
MANE Select
|
NP_057474.2:n.712+16C>T
|
|