ENST00000440460.7:c.1767C>G
MANE Select
|
ENSP00000394352.3:p.His589Gln
|
|
ENST00000440460.6:c.1767C>G
|
ENSP00000394352.3:p.His589Gln
|
|
ENST00000526500.5:n.763C>G
|
|
|
ENST00000615255.1:c.1134C>G
|
ENSP00000480808.1:p.His378Gln
|
|
ENST00000618522.4:n.1120C>G
|
|
|
NM_001037954.3:c.1767C>G
|
NP_001033043.1:p.His589Gln
|
|
NM_033425.4:c.1134C>G
|
NP_219493.1:p.His378Gln
|
|
XM_005277726.3:c.1767C>G
|
XP_005277783.1:p.His589Gln
|
|
XM_005277727.3:c.1764C>G
|
XP_005277784.1:p.His588Gln
|
|
XM_005277728.3:c.1134C>G
|
XP_005277785.1:p.His378Gln
|
|
XM_011543045.1:c.885C>G
|
XP_011541347.1:p.His295Gln
|
|
XM_011543046.1:c.879C>G
|
XP_011541348.1:p.His293Gln
|
|
XM_017018466.2:c.1764C>G
|
XP_016873955.1:p.His588Gln
|
|
XM_017018467.1:c.1764C>G
|
XP_016873956.1:p.His588Gln
|
|
XM_017018468.1:c.885C>G
|
XP_016873957.1:p.His295Gln
|
|
XM_017018469.1:c.879C>G
|
XP_016873958.1:p.His293Gln
|
|
XM_024448742.1:c.1659C>G
|
XP_024304510.1:p.His553Gln
|
|
XM_024448743.1:c.1656C>G
|
XP_024304511.1:p.His552Gln
|
|
NM_001037954.4:c.1767C>G
MANE Select
|
NP_001033043.1:p.His589Gln
|
|
NM_033425.5:c.1134C>G
|
NP_219493.1:p.His378Gln
|
|