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ENST00000405460.9:c.11562_11563insACT
MANE Select
|
ENSP00000384582.2:p.Ala3854_Glu3855insThr
|
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|
ENST00000425867.3:c.693_694insACT
|
ENSP00000392618.3:p.Ala231_Glu232insThr
|
|
|
ENST00000639431.1:c.265+78958_265+78959insACT
|
ENSP00000491057.1:n.265+78958_265+78959insACT
|
|
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ENST00000640374.1:n.4706_4707insACT
|
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|
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ENST00000640464.1:n.1981_1982insACT
|
|
|
|
ENST00000405460.6:c.11562_11563insACT
|
ENSP00000384582.2:p.Ala3854_Glu3855insThr
|
|
|
ENST00000509621.1:c.4259_4260insACT
|
|
|
|
NM_032119.3:c.11562_11563insACT
|
NP_115495.3:p.Ala3854_Glu3855insThr
|
|
|
NR_003149.1:n.11575_11576insACT
|
|
|
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XM_011543675.1:c.11559_11560insACT
|
XP_011541977.1:p.Ala3853_Glu3854insThr
|
|
|
XM_011543676.1:c.11481_11482insACT
|
XP_011541978.1:p.Ala3827_Glu3828insThr
|
|
|
XM_011543677.1:c.8865_8866insACT
|
XP_011541979.1:p.Ala2955_Glu2956insThr
|
|
|
XM_011543678.1:c.11562_11563insACT
|
XP_011541980.1:p.Ala3854_Glu3855insThr
|
|
|
NM_032119.4:c.11562_11563insACT
MANE Select
|
NP_115495.3:p.Ala3854_Glu3855insThr
|
|
|
XM_017009963.2:c.11583_11584insACT
|
XP_016865452.1:p.Ala3861_Glu3862insThr
|
|
|
XM_017009964.2:c.11580_11581insACT
|
XP_016865453.1:p.Ala3860_Glu3861insThr
|
|
|
XM_017009965.1:c.11580_11581insACT
|
XP_016865454.1:p.Ala3860_Glu3861insThr
|
|
|
XM_017009966.2:c.11502_11503insACT
|
XP_016865455.1:p.Ala3834_Glu3835insThr
|
|
|
XM_017009967.1:c.11487_11488insACT
|
XP_016865456.1:p.Ala3829_Glu3830insThr
|
|
|
XM_017009968.2:c.11583_11584insACT
|
XP_016865457.1:p.Ala3861_Glu3862insThr
|
|
|
XM_017009969.2:c.11583_11584insACT
|
XP_016865458.1:p.Ala3861_Glu3862insThr
|
|
|
XM_017009970.2:c.11583_11584insACT
|
XP_016865459.1:p.Ala3861_Glu3862insThr
|
|
|
XM_017009971.2:c.11583_11584insACT
|
XP_016865460.1:p.Ala3861_Glu3862insThr
|
|
|
XM_017009972.1:c.4701_4702insACT
|
XP_016865461.1:p.Ala1567_Glu1568insThr
|
|
|
XM_017009973.1:c.4680_4681insACT
|
XP_016865462.1:p.Ala1560_Glu1561insThr
|
|
|
NR_003149.2:n.11578_11579insACT
|
|
|
