ENST00000649276.2:c.1366C=
MANE Select
|
ENSP00000497003.1:p.His456=
|
|
ENST00000329705.11:c.1009+716C=
|
ENSP00000331176.7:n.1009+716C=
|
|
ENST00000332710.8:c.1339C=
|
ENSP00000331791.4:p.His447=
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|
ENST00000359500.7:c.1009+716C=
|
ENSP00000352483.3:n.1009+716C=
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|
ENST00000621939.1:c.1009+716C=
|
ENSP00000477982.1:n.1009+716C=
|
|
NM_005992.1:c.1009+716C=
|
NP_005983.1:n.1009+716C=
|
|
NM_080646.1:c.1009+716C=
|
NP_542377.1:n.1009+716C=
|
|
NM_080647.1:c.1339C= , LRG_226t1:c.1339C=
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NP_542378.1:p.His447=
|
|
XM_006724312.1:c.1339C=
|
XP_006724375.1:p.His447=
|
|
XM_011530351.1:c.1366C=
|
XP_011528653.1:p.His456=
|
|
XM_006724312.2:c.1339C=
|
XP_006724375.1:p.His447=
|
|
XM_017028925.1:c.1489C=
|
XP_016884414.1:p.His497=
|
|
XM_017028926.1:c.1339C=
|
XP_016884415.1:p.His447=
|
|
XM_017028927.1:c.694C=
|
XP_016884416.1:p.His232=
|
|
XM_017028928.1:c.1159+716C=
|
XP_016884417.1:n.1159+716C=
|
|
NM_001379200.1:c.1366C=
MANE Select
|
NP_001366129.1:p.His456=
|
|
NM_080646.2:c.1009+716C=
|
NP_542377.1:n.1009+716C=
|
|