ENST00000333891.14:c.14791+1776T>C
MANE Select
|
ENSP00000334319.8:n.14791+1776T>C
|
|
ENST00000333891.13:c.14791+1776T>C
|
ENSP00000334319.8:n.14791+1776T>C
|
|
ENST00000423517.6:c.*1759T>C
|
ENSP00000388393.2:n.*1759T>C
|
|
ENST00000432078.2:n.279+393T>C
|
|
|
NM_014510.2:c.*1759T>C
|
NP_055325.2:n.*1759T>C
|
|
NM_033026.5:c.14791+1776T>C
|
NP_149015.2:n.14791+1776T>C
|
|
XM_017012006.2:c.7879+393T>C
|
XP_016867495.1:n.7879+393T>C
|
|
XR_001744643.2:n.17743+393T>C
|
|
|
NM_033026.6:c.14791+1776T>C
MANE Select
|
NP_149015.2:n.14791+1776T>C
|
|
NM_014510.3:c.*1759T>C
|
NP_055325.2:n.*1759T>C
|
|