ENST00000254108.12:c.*80T>A
MANE Select
|
ENSP00000254108.8:n.*80T>A
|
|
ENST00000254108.11:c.*80T>A
|
ENSP00000254108.7:n.*80T>A
|
|
ENST00000380244.7:c.*80T>A
|
ENSP00000369594.3:n.*80T>A
|
|
ENST00000483853.1:n.738T>A
|
|
|
ENST00000487509.6:n.4836T>A
|
|
|
ENST00000566605.5:c.*834T>A
|
ENSP00000455073.1:n.*834T>A
|
|
ENST00000568685.1:c.*80T>A
|
ENSP00000455282.1:n.*80T>A
|
|
ENST00000569760.5:n.552T>A
|
|
|
NM_001170634.1:c.*80T>A
|
NP_001164105.1:n.*80T>A
|
|
NM_001170937.1:c.*80T>A
|
NP_001164408.1:n.*80T>A
|
|
NM_004960.3:c.*80T>A , LRG_655t1:c.*80T>A
|
NP_004951.1:n.*80T>A
|
|
NR_028388.2:n.1731T>A
|
|
|
XM_005255233.3:c.*80T>A
|
XP_005255290.1:n.*80T>A
|
|
XM_011545781.1:c.*80T>A
|
XP_011544083.1:n.*80T>A
|
|
XM_011545782.1:c.*80T>A
|
XP_011544084.1:n.*80T>A
|
|
XM_005255233.5:c.*80T>A
|
XP_005255290.1:n.*80T>A
|
|
XM_011545782.2:c.*80T>A
|
XP_011544084.1:n.*80T>A
|
|
XM_024450221.1:c.*80T>A
|
XP_024305989.1:n.*80T>A
|
|
NM_004960.4:c.*80T>A
MANE Select
|
NP_004951.1:n.*80T>A
|
|