ENST00000261842.10:c.2350G>T
MANE Select
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ENSP00000261842.5:p.Gly784Ter
|
|
ENST00000261842.9:c.2350G>T
|
ENSP00000261842.5:p.Gly784Ter
|
|
ENST00000558439.5:c.*1474G>T
|
ENSP00000452712.1:n.*1474G>T
|
|
ENST00000560508.1:c.2125G>T
|
ENSP00000452976.1:p.Gly709Ter
|
|
ENST00000561393.5:c.*1394G>T
|
ENSP00000452711.1:n.*1394G>T
|
|
NM_001252127.1:c.2125G>T
|
NP_001239056.1:p.Gly709Ter
|
|
NM_007347.4:c.2350G>T
|
NP_031373.2:p.Gly784Ter
|
|
XM_005254264.2:c.2125G>T
|
XP_005254321.1:p.Gly709Ter
|
|
XM_006720447.2:c.2125G>T
|
XP_006720510.1:p.Gly709Ter
|
|
XM_011521408.1:c.2170G>T
|
XP_011519710.1:p.Gly724Ter
|
|
XM_011521409.1:c.1000G>T
|
XP_011519711.1:p.Gly334Ter
|
|
XM_005254264.4:c.2125G>T
|
XP_005254321.1:p.Gly709Ter
|
|
XM_006720447.4:c.2125G>T
|
XP_006720510.1:p.Gly709Ter
|
|
XM_017022042.2:c.1468G>T
|
XP_016877531.1:p.Gly490Ter
|
|
XR_001751183.1:n.2457G>T
|
|
|
XR_001751184.1:n.2333G>T
|
|
|
NM_007347.5:c.2350G>T
MANE Select
|
NP_031373.2:p.Gly784Ter
|
|
NM_001252127.2:c.2125G>T
|
NP_001239056.1:p.Gly709Ter
|
|