ENST00000602795.6:c.340+184C>T
(NELFCD)
|
ENSP00000473290.1:n.340+184C>T
|
|
ENST00000652272.2:c.286+184C>T
(NELFCD)
MANE Select
|
ENSP00000499018.1:n.286+184C>T
|
|
ENST00000681011.1:c.*8602G>A
(CTSZ)
|
ENSP00000505520.1:n.*8602G>A
|
|
ENST00000344018.7:c.313+184C>T
(NELFCD)
|
ENSP00000342300.3:n.313+184C>T
|
|
ENST00000460601.5:c.321+184C>T
(NELFCD)
|
|
|
ENST00000471621.5:n.528C>T
(NELFCD)
|
|
|
ENST00000482747.1:n.321+184C>T
(NELFCD)
|
|
|
ENST00000492016.5:n.344+184C>T
(NELFCD)
|
|
|
ENST00000602795.5:c.340+184C>T
(NELFCD)
|
ENSP00000473290.1:n.340+184C>T
|
|
NM_198976.2:c.340+184C>T
(NELFCD)
|
NP_945327.2:n.340+184C>T
|
|
XM_011528849.1:c.-328+184C>T
(NELFCD)
|
XP_011527151.1:n.-328+184C>T
|
|
XR_244142.2:n.344+184C>T
(NELFCD)
|
|
|
NM_198976.3:c.286+184C>T
(NELFCD)
|
NP_945327.3:n.286+184C>T
|
|
XR_244142.3:n.344+184C>T
(NELFCD)
|
|
|
NM_198976.4:c.286+184C>T
(NELFCD)
MANE Select
|
NP_945327.3:n.286+184C>T
|
|