ENST00000389857.11:c.4700-133G>T
MANE Select
|
ENSP00000374507.6:n.4700-133G>T
|
|
ENST00000331194.8:c.272-133G>T
|
ENSP00000330332.8:n.272-133G>T
|
|
ENST00000334448.5:n.512-133G>T
|
|
|
ENST00000389857.10:c.4700-133G>T
|
ENSP00000374507.6:n.4700-133G>T
|
|
ENST00000556726.5:c.928-133G>T
|
|
|
ENST00000557455.1:n.539G>T
|
|
|
NM_001080414.3:c.4700-133G>T
|
NP_001073883.2:n.4700-133G>T
|
|
XM_011536796.1:c.4592-133G>T
|
XP_011535098.1:n.4592-133G>T
|
|
XR_429316.2:n.4975-133G>T
|
|
|
XR_943459.1:n.5450G>T
|
|
|
XM_011536796.2:c.4592-133G>T
|
XP_011535098.1:n.4592-133G>T
|
|
XM_017021335.2:c.*441G>T
|
XP_016876824.1:n.*441G>T
|
|
XM_017021336.1:c.1781-133G>T
|
XP_016876825.1:n.1781-133G>T
|
|
XR_429316.4:n.4973-133G>T
|
|
|
NM_001080414.4:c.4700-133G>T
MANE Select
|
NP_001073883.2:n.4700-133G>T
|
|