ENST00000647814.1:c.3987+119C>T
MANE Select
|
ENSP00000497274.1:n.3987+119C>T
|
|
ENST00000649459.1:n.335+119C>T
|
|
|
ENST00000370449.8:c.3987+119C>T
|
ENSP00000359478.4:n.3987+119C>T
|
|
NM_000392.4:c.3987+119C>T
|
NP_000383.1:n.3987+119C>T
|
|
XM_006717630.2:c.3291+119C>T
|
XP_006717693.1:n.3291+119C>T
|
|
XR_945604.1:n.4176+119C>T
|
|
|
XR_945605.1:n.4051+119C>T
|
|
|
NM_000392.5:c.3987+119C>T
MANE Select
|
NP_000383.2:n.3987+119C>T
|
|
XM_006717630.3:c.3291+119C>T
|
XP_006717693.1:n.3291+119C>T
|
|
XR_945604.3:n.4230+119C>T
|
|
|
XR_945605.3:n.4103+119C>T
|
|
|