ENST00000403665.7:c.1339G>C
MANE Select
|
ENSP00000384957.2:p.Gly447Arg
|
|
ENST00000264691.4:c.35G>C
|
|
|
ENST00000264692.8:c.1177G>C
|
ENSP00000264692.5:p.Gly393Arg
|
|
ENST00000403665.6:c.1339G>C
|
ENSP00000384957.2:p.Gly447Arg
|
|
NM_000128.3:c.1339G>C , LRG_583t1:c.1339G>C
|
NP_000119.1:p.Gly447Arg
|
|
XM_005262821.2:c.1342G>C
|
XP_005262878.1:p.Gly448Arg
|
|
XM_005262822.2:c.1342G>C
|
XP_005262879.1:p.Gly448Arg
|
|
XM_005262823.2:c.1072G>C
|
XP_005262880.1:p.Gly358Arg
|
|
XM_005262824.1:c.1342G>C
|
XP_005262881.1:p.Gly448Arg
|
|
XM_006714137.1:c.1294G>C
|
XP_006714200.1:p.Gly432Arg
|
|
XR_938706.1:n.1747G>C
|
|
|
XR_938707.1:n.1747G>C
|
|
|
XM_005262821.4:c.1342G>C
|
XP_005262878.1:p.Gly448Arg
|
|
XM_005262822.4:c.1342G>C
|
XP_005262879.1:p.Gly448Arg
|
|
XM_005262823.4:c.1072G>C
|
XP_005262880.1:p.Gly358Arg
|
|
XM_006714137.3:c.1294G>C
|
XP_006714200.1:p.Gly432Arg
|
|
XR_001741172.2:n.1813G>C
|
|
|
NM_000128.4:c.1339G>C
MANE Select
|
NP_000119.1:p.Gly447Arg
|
|