ENST00000327892.13:c.1186C>T
MANE Select
|
ENSP00000339001.7:p.His396Tyr
|
|
ENST00000680530.1:n.2048C>T
|
|
|
ENST00000681421.1:n.2252C>T
|
|
|
ENST00000681435.1:c.970C>T
|
ENSP00000506665.1:p.His324Tyr
|
|
ENST00000327892.12:c.1186C>T
|
ENSP00000339001.7:p.His396Tyr
|
|
ENST00000330914.7:c.970C>T
|
ENSP00000365578.2:p.His324Tyr
|
|
ENST00000396384.1:c.970C>T
|
ENSP00000379668.1:p.His324Tyr
|
|
ENST00000396389.5:c.1132C>T
|
ENSP00000379672.1:p.His378Tyr
|
|
NM_001293212.1:c.1246C>T
|
NP_001280141.1:p.His416Tyr
|
|
NM_001293213.1:c.580C>T
|
NP_001280142.1:p.His194Tyr
|
|
NM_001293214.1:c.1054C>T
|
NP_001280143.1:p.His352Tyr
|
|
NM_001293215.1:c.970C>T
|
NP_001280144.1:p.His324Tyr
|
|
NM_001293216.1:c.970C>T
|
NP_001280145.1:p.His324Tyr
|
|
NM_178014.3:c.1186C>T
|
NP_821133.1:p.His396Tyr
|
|
NR_120608.1:n.893C>T
|
|
|
NM_178014.4:c.1186C>T
MANE Select
|
NP_821133.1:p.His396Tyr
|
|
NM_001293212.2:c.1246C>T
|
NP_001280141.1:p.His416Tyr
|
|
NM_001293213.2:c.580C>T
|
NP_001280142.1:p.His194Tyr
|
|
NM_001293214.2:c.1054C>T
|
NP_001280143.1:p.His352Tyr
|
|
NM_001293215.2:c.970C>T
|
NP_001280144.1:p.His324Tyr
|
|
NM_001293216.2:c.970C>T
|
NP_001280145.1:p.His324Tyr
|
|
NR_120608.2:n.742C>T
|
|
|