ENST00000470094.2:c.*522T=
|
ENSP00000434898.2:n.*522T=
|
|
ENST00000528762.2:c.*1366T=
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ENSP00000433168.2:n.*1366T=
|
|
ENST00000530893.7:c.9630T=
|
ENSP00000499438.2:p.Leu3210=
|
|
ENST00000665585.2:c.*1561T=
|
ENSP00000499570.2:n.*1561T=
|
|
ENST00000700202.2:c.9948T=
|
ENSP00000514856.2:p.Leu3316=
|
|
ENST00000700202.1:c.2415T=
|
ENSP00000514856.1:p.Leu805=
|
|
ENST00000700203.1:n.2126T=
|
|
|
ENST00000380152.8:c.9999T=
MANE Select
|
ENSP00000369497.3:p.Leu3333=
|
|
ENST00000544455.6:c.9999T=
|
ENSP00000439902.1:p.Leu3333=
|
|
ENST00000614259.2:c.10007T=
|
ENSP00000506251.1:n.10007T=
|
|
ENST00000680887.1:c.9999T=
|
ENSP00000505508.1:p.Leu3333=
|
|
ENST00000380152.7:c.9999T=
|
ENSP00000369497.3:p.Leu3333=
|
|
ENST00000544455.5:c.9999T=
|
ENSP00000439902.1:p.Leu3333=
|
|
NM_000059.3:c.9999T= , LRG_293t1:c.9999T=
|
NP_000050.2:p.Leu3333=
|
|
XM_011535203.1:c.9999T=
|
XP_011533505.1:p.Leu3333=
|
|
XM_011535204.1:c.9903T=
|
XP_011533506.1:p.Leu3301=
|
|
NM_000059.4:c.9999T=
MANE Select
|
NP_000050.3:p.Leu3333=
|
|