ENST00000325455.10:c.*4386G>T
MANE Select
|
ENSP00000325120.5:n.*4386G>T
|
|
ENST00000325455.9:c.*4386G>T
|
ENSP00000325120.5:n.*4386G>T
|
|
NM_000926.4:c.*4386G>T
MANE Select
|
NP_000917.3:n.*4386G>T
|
|
NM_001202474.3:c.*4386G>T
|
NP_001189403.1:n.*4386G>T
|
|
NM_001271161.2:c.*4386G>T
|
NP_001258090.1:n.*4386G>T
|
|
NM_001271162.1:c.*4386G>T
|
NP_001258091.1:n.*4386G>T
|
|
NR_073141.2:n.7129G>T
|
|
|
NR_073142.2:n.7012G>T
|
|
|
NR_073143.2:n.6744G>T
|
|
|
NM_001271162.2:c.*4386G>T
|
NP_001258091.1:n.*4386G>T
|
|
NR_073141.3:n.7143G>T
|
|
|
NR_073142.3:n.7026G>T
|
|
|
NR_073143.3:n.6758G>T
|
|
|