ENST00000298910.12:c.7030T>A
MANE Select
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ENSP00000298910.7:p.Phe2344Ile
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ENST00000636518.1:c.827T>A
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ENST00000679360.1:c.*5939T>A
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ENSP00000505368.1:n.*5939T>A
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ENST00000679532.1:c.2804T>A
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|
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ENST00000679683.1:c.820T>A
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ENST00000680018.1:c.2475T>A
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ENSP00000505347.1:n.2475T>A
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ENST00000680422.1:c.4117T>A
|
|
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ENST00000680425.1:c.2197T>A
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ENSP00000506459.1:n.2197T>A
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ENST00000680453.1:c.2487T>A
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ENST00000680790.1:c.6775T>A
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ENSP00000505335.1:p.Phe2259Ile
|
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ENST00000681136.1:n.3014T>A
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|
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ENST00000681696.1:c.2713T>A
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ENSP00000505871.1:p.Phe905Ile
|
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ENST00000681773.1:n.237T>A
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|
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ENST00000298910.11:c.7030T>A
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ENSP00000298910.7:p.Phe2344Ile
|
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ENST00000430804.5:c.4326T>A
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|
|
ENST00000479187.5:n.3711T>A
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NM_198578.3:c.7030T>A
|
NP_940980.3:p.Phe2344Ile
|
|
XM_005268629.2:c.7030T>A
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XP_005268686.1:p.Phe2344Ile
|
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XM_011537877.1:c.7030T>A
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XP_011536179.1:p.Phe2344Ile
|
|
XM_011537879.1:c.5827T>A
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XP_011536181.1:p.Phe1943Ile
|
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XR_944868.1:n.485-8576A>T
|
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XM_005268629.4:c.7030T>A
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XP_005268686.1:p.Phe2344Ile
|
|
XM_011537877.3:c.7030T>A
|
XP_011536179.1:p.Phe2344Ile
|
|
XM_017018787.1:c.3946T>A
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XP_016874276.1:p.Phe1316Ile
|
|
XM_017018788.2:c.3292T>A
|
XP_016874277.1:p.Phe1098Ile
|
|
XM_024448833.1:c.5827T>A
|
XP_024304601.1:p.Phe1943Ile
|
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XR_944868.2:n.485-8576A>T
|
|
|
NM_198578.4:c.7030T>A
MANE Select
|
NP_940980.4:p.Phe2344Ile
|
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