ENST00000448821.6:c.1290G=
|
ENSP00000402902.2:p.Gly430=
|
|
ENST00000685871.1:c.1290G=
|
ENSP00000509964.1:p.Gly430=
|
|
ENST00000686159.1:n.1329G=
|
|
|
ENST00000686486.1:n.298G=
|
|
|
ENST00000687302.1:n.1376G=
|
|
|
ENST00000687357.1:c.1290G=
|
ENSP00000509549.1:p.Gly430=
|
|
ENST00000687625.1:n.445G=
|
|
|
ENST00000687787.1:c.1290G=
|
ENSP00000509440.1:p.Gly430=
|
|
ENST00000688201.1:n.1322G=
|
|
|
ENST00000688226.1:n.1222G=
|
|
|
ENST00000688869.1:n.1596G=
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|
|
ENST00000689788.1:c.1084G=
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ENSP00000508973.1:n.1084G=
|
|
ENST00000689898.1:c.1290G=
|
ENSP00000509651.1:p.Gly430=
|
|
ENST00000690070.1:c.1290G=
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ENSP00000509654.1:p.Gly430=
|
|
ENST00000690267.1:c.1154G=
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ENSP00000510432.1:n.1154G=
|
|
ENST00000690552.1:n.1151G=
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|
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ENST00000691138.1:n.1151G=
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|
|
ENST00000691969.1:c.865G=
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ENSP00000510244.1:n.865G=
|
|
ENST00000692232.1:n.2446G=
|
|
|
ENST00000692233.1:c.1154G=
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ENSP00000509698.1:n.1154G=
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|
ENST00000692380.1:n.445G=
|
|
|
ENST00000692447.1:n.2402G=
|
|
|
ENST00000693094.1:c.1290G=
|
ENSP00000510161.1:p.Gly430=
|
|
ENST00000342694.7:c.1290G=
MANE Select
|
ENSP00000341083.2:p.Gly430=
|
|
ENST00000342694.6:c.1290G=
|
ENSP00000341083.2:p.Gly430=
|
|
ENST00000464810.5:n.1290G=
|
|
|
NM_003995.3:c.1290G=
|
NP_003986.2:p.Gly430=
|
|
XM_005251478.3:c.1290G=
|
XP_005251535.1:p.Gly430=
|
|
XM_005251479.3:c.303G=
|
XP_005251536.1:p.Gly101=
|
|
XM_006716778.2:c.1290G=
|
XP_006716841.1:p.Gly430=
|
|
XM_011517889.1:c.303G=
|
XP_011516191.1:p.Gly101=
|
|
XM_011517890.1:c.303G=
|
XP_011516192.1:p.Gly101=
|
|
XM_011517891.1:c.303G=
|
XP_011516193.1:p.Gly101=
|
|
XM_011517892.1:c.303G=
|
XP_011516194.1:p.Gly101=
|
|
XM_011517893.1:c.303G=
|
XP_011516195.1:p.Gly101=
|
|
XM_011517894.1:c.303G=
|
XP_011516196.1:p.Gly101=
|
|
XM_011517895.1:c.-119G=
|
XP_011516197.1:n.-119G=
|
|
XM_024447556.1:c.1290G=
|
XP_024303324.1:p.Gly430=
|
|
XM_024447557.1:c.1290G=
|
XP_024303325.1:p.Gly430=
|
|
XM_024447558.1:c.303G=
|
XP_024303326.1:p.Gly101=
|
|
XM_024447559.1:c.-119G=
|
XP_024303327.1:n.-119G=
|
|
XM_024447560.1:c.-119G=
|
XP_024303328.1:n.-119G=
|
|
XM_024447561.1:c.-119G=
|
XP_024303329.1:n.-119G=
|
|
NM_003995.4:c.1290G=
MANE Select
|
NP_003986.2:p.Gly430=
|
|
NM_001378923.1:c.1290G=
|
NP_001365852.1:p.Gly430=
|
|