ENST00000357749.7:c.1165A>T
MANE Select
|
ENSP00000350386.2:p.Arg389Trp
|
|
ENST00000357749.6:c.1165A>T
|
ENSP00000350386.2:p.Arg389Trp
|
|
ENST00000467744.2:n.126+71337A>T
|
|
|
NM_000390.2:c.1165A>T , LRG_699t1:c.1165A>T
|
NP_000381.1:p.Arg389Trp
|
|
XM_006724615.2:c.1102A>T
|
XP_006724678.1:p.Arg368Trp
|
|
XM_011530839.1:c.721A>T
|
XP_011529141.1:p.Arg241Trp
|
|
NM_000390.3:c.1165A>T
|
NP_000381.1:p.Arg389Trp
|
|
NM_001320959.1:c.721A>T
|
NP_001307888.1:p.Arg241Trp
|
|
NM_001362517.1:c.721A>T
|
NP_001349446.1:p.Arg241Trp
|
|
NM_001362518.1:c.721A>T
|
NP_001349447.1:p.Arg241Trp
|
|
NM_001362519.1:c.721A>T
|
NP_001349448.1:p.Arg241Trp
|
|
XM_017029242.2:c.1165A>T
|
XP_016884731.1:p.Arg389Trp
|
|
XM_017029246.1:c.721A>T
|
XP_016884735.1:p.Arg241Trp
|
|
XM_024452331.1:c.721A>T
|
XP_024308099.1:p.Arg241Trp
|
|
NM_000390.4:c.1165A>T
MANE Select
|
NP_000381.1:p.Arg389Trp
|
|
NM_001362518.2:c.721A>T
|
NP_001349447.1:p.Arg241Trp
|
|