ENST00000254108.12:c.936+117T>C
MANE Select
|
ENSP00000254108.8:n.936+117T>C
|
|
ENST00000254108.11:c.936+117T>C
|
ENSP00000254108.7:n.936+117T>C
|
|
ENST00000380244.7:c.933+117T>C
|
ENSP00000369594.3:n.933+117T>C
|
|
ENST00000474990.5:n.230+117T>C
|
|
|
ENST00000487509.6:n.4111+117T>C
|
|
|
ENST00000564766.1:n.760+117T>C
|
|
|
ENST00000566605.5:c.*109+117T>C
|
ENSP00000455073.1:n.*109+117T>C
|
|
ENST00000568685.1:c.939+117T>C
|
ENSP00000455282.1:n.939+117T>C
|
|
ENST00000568901.2:n.310+117T>C
|
|
|
NM_001170634.1:c.933+117T>C
|
NP_001164105.1:n.933+117T>C
|
|
NM_001170937.1:c.924+117T>C
|
NP_001164408.1:n.924+117T>C
|
|
NM_004960.3:c.936+117T>C , LRG_655t1:c.936+117T>C
|
NP_004951.1:n.936+117T>C
|
|
NR_028388.2:n.1006+117T>C
|
|
|
XM_005255233.3:c.321+117T>C
|
XP_005255290.1:n.321+117T>C
|
|
XM_011545781.1:c.930+117T>C
|
XP_011544083.1:n.930+117T>C
|
|
XM_011545782.1:c.321+117T>C
|
XP_011544084.1:n.321+117T>C
|
|
XM_005255233.5:c.321+117T>C
|
XP_005255290.1:n.321+117T>C
|
|
XM_011545782.2:c.321+117T>C
|
XP_011544084.1:n.321+117T>C
|
|
XM_024450221.1:c.927+117T>C
|
XP_024305989.1:n.927+117T>C
|
|
NM_004960.4:c.936+117T>C
MANE Select
|
NP_004951.1:n.936+117T>C
|
|