ENST00000284268.8:c.1141+322A>C
(ANKH)
MANE Select
|
ENSP00000284268.6:n.1141+322A>C
|
|
ENST00000284268.6:c.1141+322A>C
(ANKH)
|
ENSP00000284268.6:n.1141+322A>C
|
|
ENST00000502585.1:n.383+322A>C
(ANKH)
|
|
|
NM_054027.4:c.1141+322A>C
(ANKH)
|
NP_473368.1:n.1141+322A>C
|
|
NR_046285.1:n.2492-38T>G
|
|
|
NM_054027.5:c.1141+322A>C
(ANKH)
|
NP_473368.1:n.1141+322A>C
|
|
XM_011514151.2:c.*3709T>G
(OTULIN)
|
XP_011512453.1:n.*3709T>G
|
|
XM_017009644.2:c.1057+322A>C
(ANKH)
|
XP_016865133.1:n.1057+322A>C
|
|
NM_054027.6:c.1141+322A>C
(ANKH)
MANE Select
|
NP_473368.1:n.1141+322A>C
|
|