ENST00000684583.1:c.*2968G>T
(AHRR)
MANE Select
|
ENSP00000507476.1:n.*2968G>T
|
|
ENST00000316418.10:c.*2968G>T
(AHRR)
|
ENSP00000323816.6:n.*2968G>T
|
|
ENST00000505113.6:c.*5058G>T
(PDCD6-AHRR)
|
ENSP00000424601.2:n.*5058G>T
|
|
ENST00000675395.1:c.*5112G>T
(PDCD6-AHRR)
|
ENSP00000502570.1:n.*5112G>T
|
|
ENST00000316418.9:c.*2968G>T
(AHRR)
|
ENSP00000323816.5:n.*2968G>T
|
|
NM_001242412.1:c.*2968G>T
(AHRR)
|
NP_001229341.1:n.*2968G>T
|
|
NM_020731.4:c.*2968G>T
(AHRR)
|
NP_065782.2:n.*2968G>T
|
|
NM_001377236.1:c.*2968G>T
(AHRR)
MANE Select
|
NP_001364165.1:n.*2968G>T
|
|
NM_001377239.1:c.*2968G>T
(AHRR)
|
NP_001364168.1:n.*2968G>T
|
|
NR_165159.2:n.5409G>T
(PDCD6-AHRR)
|
|
|
NR_165163.2:n.5355G>T
(PDCD6-AHRR)
|
|
|