ENST00000403665.7:c.1129G>C
MANE Select
|
ENSP00000384957.2:p.Asp377His
|
|
ENST00000264692.8:c.967G>C
|
ENSP00000264692.5:p.Asp323His
|
|
ENST00000403665.6:c.1129G>C
|
ENSP00000384957.2:p.Asp377His
|
|
ENST00000452239.1:c.576G>C
|
|
|
NM_000128.3:c.1129G>C , LRG_583t1:c.1129G>C
|
NP_000119.1:p.Asp377His
|
|
XM_005262821.2:c.1132G>C
|
XP_005262878.1:p.Asp378His
|
|
XM_005262822.2:c.1132G>C
|
XP_005262879.1:p.Asp378His
|
|
XM_005262823.2:c.862G>C
|
XP_005262880.1:p.Asp288His
|
|
XM_005262824.1:c.1132G>C
|
XP_005262881.1:p.Asp378His
|
|
XM_006714137.1:c.1084G>C
|
XP_006714200.1:p.Asp362His
|
|
XR_938706.1:n.1484G>C
|
|
|
XR_938707.1:n.1484G>C
|
|
|
XM_005262821.4:c.1132G>C
|
XP_005262878.1:p.Asp378His
|
|
XM_005262822.4:c.1132G>C
|
XP_005262879.1:p.Asp378His
|
|
XM_005262823.4:c.862G>C
|
XP_005262880.1:p.Asp288His
|
|
XM_006714137.3:c.1084G>C
|
XP_006714200.1:p.Asp362His
|
|
XM_017007884.2:c.1132G>C
|
XP_016863373.1:p.Asp378His
|
|
XM_017007885.2:c.1132G>C
|
XP_016863374.1:p.Asp378His
|
|
XM_017007886.2:c.1129G>C
|
XP_016863375.1:p.Asp377His
|
|
XR_001741172.2:n.1550G>C
|
|
|
NM_000128.4:c.1129G>C
MANE Select
|
NP_000119.1:p.Asp377His
|
|