ENST00000263207.8:c.2534C>G
MANE Select
|
ENSP00000263207.3:p.Thr845Ser
|
|
ENST00000263207.7:c.2534C>G
|
ENSP00000263207.3:p.Thr845Ser
|
|
ENST00000401994.5:c.2345C>G
|
ENSP00000384341.1:p.Thr782Ser
|
|
ENST00000406259.1:c.2516C>G
|
ENSP00000385444.1:p.Thr839Ser
|
|
ENST00000406522.5:c.2327C>G
|
ENSP00000384732.1:p.Thr776Ser
|
|
ENST00000495096.5:n.1456C>G
|
|
|
NM_001670.2:c.2534C>G
|
NP_001661.1:p.Thr845Ser
|
|
XM_005261242.1:c.2516C>G
|
XP_005261299.1:p.Thr839Ser
|
|
XM_005261243.3:c.2516C>G
|
XP_005261300.1:p.Thr839Ser
|
|
XM_005261244.3:c.2516C>G
|
XP_005261301.1:p.Thr839Ser
|
|
XM_006724243.1:c.2534C>G
|
XP_006724306.1:p.Thr845Ser
|
|
XM_006724245.2:c.2534C>G
|
XP_006724308.1:p.Thr845Ser
|
|
XM_006724246.2:c.2288C>G
|
XP_006724309.1:p.Thr763Ser
|
|
XM_006724247.2:c.2345C>G
|
XP_006724310.1:p.Thr782Ser
|
|
XM_006724248.2:c.2327C>G
|
XP_006724311.1:p.Thr776Ser
|
|
XM_011530179.1:c.2501C>G
|
XP_011528481.1:p.Thr834Ser
|
|
XM_011530180.1:c.2534C>G
|
XP_011528482.1:p.Thr845Ser
|
|
XM_011530182.1:c.1100C>G
|
XP_011528484.1:p.Thr367Ser
|
|
XM_011530183.1:c.1082C>G
|
XP_011528485.1:p.Thr361Ser
|
|
XR_937863.1:n.2621C>G
|
|
|
XR_937864.1:n.2621C>G
|
|
|
XM_005261242.3:c.2516C>G
|
XP_005261299.1:p.Thr839Ser
|
|
XM_005261243.4:c.2516C>G
|
XP_005261300.1:p.Thr839Ser
|
|
XM_005261244.4:c.2516C>G
|
XP_005261301.1:p.Thr839Ser
|
|
XM_006724243.3:c.2534C>G
|
XP_006724306.1:p.Thr845Ser
|
|
XM_006724245.3:c.2534C>G
|
XP_006724308.1:p.Thr845Ser
|
|
XM_006724246.4:c.2288C>G
|
XP_006724309.1:p.Thr763Ser
|
|
XM_006724247.4:c.2345C>G
|
XP_006724310.1:p.Thr782Ser
|
|
XM_006724248.4:c.2327C>G
|
XP_006724311.1:p.Thr776Ser
|
|
XM_011530179.3:c.2501C>G
|
XP_011528481.1:p.Thr834Ser
|
|
XM_011530182.3:c.1100C>G
|
XP_011528484.1:p.Thr367Ser
|
|
XM_011530183.3:c.1082C>G
|
XP_011528485.1:p.Thr361Ser
|
|
XM_024452249.1:c.2288C>G
|
XP_024308017.1:p.Thr763Ser
|
|
XR_937863.2:n.2621C>G
|
|
|
NM_001670.3:c.2534C>G
MANE Select
|
NP_001661.1:p.Thr845Ser
|
|