ENST00000350721.9:c.6308A=
MANE Select
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ENSP00000343741.4:p.Glu2103=
|
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ENST00000513291.2:n.1492A=
|
|
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ENST00000654170.1:n.1151A=
|
|
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ENST00000656590.1:c.5098A=
|
|
|
ENST00000661310.1:c.6116A=
|
ENSP00000499589.1:p.Glu2039=
|
|
ENST00000665483.1:n.163A=
|
|
|
ENST00000666447.1:n.143A=
|
|
|
ENST00000666943.1:n.1772A=
|
|
|
ENST00000350721.8:c.6308A=
|
ENSP00000343741.4:p.Glu2103=
|
|
NM_001184.3:c.6308A=
|
NP_001175.2:p.Glu2103=
|
|
XM_011512924.1:c.6314A=
|
XP_011511226.1:p.Glu2105=
|
|
XM_011512925.1:c.6122A=
|
XP_011511227.1:p.Glu2041=
|
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XR_924147.1:n.6403A=
|
|
|
XR_924148.1:n.6403A=
|
|
|
XR_924149.1:n.6282A=
|
|
|
NM_001354579.1:c.6116A=
|
NP_001341508.1:p.Glu2039=
|
|
XR_001740179.2:n.6397A=
|
|
|
XR_001740180.2:n.6451A=
|
|
|
XR_001740181.2:n.6330A=
|
|
|
XR_001740182.1:n.6282A=
|
|
|
XR_002959543.1:n.6507A=
|
|
|
XR_924148.2:n.6403A=
|
|
|
NM_001184.4:c.6308A=
MANE Select
|
NP_001175.2:p.Glu2103=
|
|
NM_001354579.2:c.6116A=
|
NP_001341508.1:p.Glu2039=
|
|