ENST00000233072.10:c.1164+302T>C
MANE Select
|
ENSP00000233072.5:n.1164+302T>C
|
|
ENST00000430249.7:c.1182+302T>C
|
ENSP00000402608.2:n.1182+302T>C
|
|
ENST00000673510.1:c.1164+302T>C
|
ENSP00000500537.1:n.1164+302T>C
|
|
ENST00000673630.1:c.1164+302T>C
|
ENSP00000501073.1:n.1164+302T>C
|
|
ENST00000673711.1:c.1164+302T>C
|
ENSP00000501022.1:n.1164+302T>C
|
|
ENST00000233072.9:c.1164+302T>C
|
ENSP00000233072.5:n.1164+302T>C
|
|
ENST00000430249.6:c.1182+302T>C
|
ENSP00000402608.2:n.1182+302T>C
|
|
ENST00000619804.1:c.1164+302T>C
|
ENSP00000480517.1:n.1164+302T>C
|
|
NM_001122633.2:c.1182+302T>C
|
NP_001116105.1:n.1182+302T>C
|
|
NM_001875.4:c.1164+302T>C , LRG_336t1:c.1164+302T>C
|
NP_001866.2:n.1164+302T>C
|
|
XM_011510640.1:c.1197+302T>C
|
XP_011508942.1:n.1197+302T>C
|
|
XM_011510641.1:c.1164+302T>C
|
XP_011508943.1:n.1164+302T>C
|
|
XM_011510642.1:c.1164+302T>C
|
XP_011508944.1:n.1164+302T>C
|
|
XM_011510643.1:c.1164+302T>C
|
XP_011508945.1:n.1164+302T>C
|
|
XM_011510644.1:c.1164+302T>C
|
XP_011508946.1:n.1164+302T>C
|
|
NM_001122633.3:c.1164+302T>C
|
NP_001116105.2:n.1164+302T>C
|
|
NM_001369256.1:c.1197+302T>C
|
NP_001356185.1:n.1197+302T>C
|
|
NM_001369257.1:c.1164+302T>C
|
NP_001356186.1:n.1164+302T>C
|
|
NM_001875.5:c.1164+302T>C
MANE Select
|
NP_001866.2:n.1164+302T>C
|
|
NR_161225.1:n.2076+302T>C
|
|
|