ENST00000403665.7:c.1157C>A
MANE Select
|
ENSP00000384957.2:p.Pro386His
|
|
ENST00000264692.8:c.995C>A
|
ENSP00000264692.5:p.Pro332His
|
|
ENST00000403665.6:c.1157C>A
|
ENSP00000384957.2:p.Pro386His
|
|
NM_000128.3:c.1157C>A , LRG_583t1:c.1157C>A
|
NP_000119.1:p.Pro386His
|
|
XM_005262821.2:c.1160C>A
|
XP_005262878.1:p.Pro387His
|
|
XM_005262822.2:c.1160C>A
|
XP_005262879.1:p.Pro387His
|
|
XM_005262823.2:c.890C>A
|
XP_005262880.1:p.Pro297His
|
|
XM_005262824.1:c.1160C>A
|
XP_005262881.1:p.Pro387His
|
|
XM_006714137.1:c.1112C>A
|
XP_006714200.1:p.Pro371His
|
|
XR_938706.1:n.1565C>A
|
|
|
XR_938707.1:n.1565C>A
|
|
|
XM_005262821.4:c.1160C>A
|
XP_005262878.1:p.Pro387His
|
|
XM_005262822.4:c.1160C>A
|
XP_005262879.1:p.Pro387His
|
|
XM_005262823.4:c.890C>A
|
XP_005262880.1:p.Pro297His
|
|
XM_006714137.3:c.1112C>A
|
XP_006714200.1:p.Pro371His
|
|
XM_017007884.2:c.*2129C>A
|
XP_016863373.1:n.*2129C>A
|
|
XM_017007885.2:c.*25C>A
|
XP_016863374.1:n.*25C>A
|
|
XR_001741172.2:n.1631C>A
|
|
|
NM_000128.4:c.1157C>A
MANE Select
|
NP_000119.1:p.Pro386His
|
|