ENST00000621392.5:c.733A=
MANE Select
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ENSP00000477573.2:p.Ile245=
|
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ENST00000315184.9:c.733A=
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ENSP00000326652.4:p.Ile245=
|
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ENST00000466842.1:c.301A=
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ENSP00000417930.1:p.Ile101=
|
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ENST00000469348.5:n.592A=
|
|
|
ENST00000471558.5:c.733A=
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ENSP00000418672.1:p.Ile245=
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|
ENST00000484425.6:c.304A=
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ENSP00000418591.2:p.Ile102=
|
|
ENST00000485070.5:c.436A=
|
ENSP00000418192.1:p.Ile146=
|
|
ENST00000493738.5:n.689A=
|
|
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ENST00000621392.4:c.436A=
|
ENSP00000477573.1:p.Ile146=
|
|
NM_001282788.1:c.733A=
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NP_001269717.1:p.Ile245=
|
|
NM_001282789.1:c.436A=
|
NP_001269718.1:p.Ile146=
|
|
NM_032599.3:c.733A=
|
NP_115988.1:p.Ile245=
|
|
NR_104242.1:n.833A=
|
|
|
NR_104243.1:n.722A=
|
|
|
XM_017012743.2:c.733A=
|
XP_016868232.1:p.Ile245=
|
|
XR_002956499.1:n.784A=
|
|
|
NM_001282788.2:c.733A=
|
NP_001269717.1:p.Ile245=
|
|
NM_001282789.2:c.436A=
|
NP_001269718.1:p.Ile146=
|
|
NM_032599.4:c.733A=
|
NP_115988.1:p.Ile245=
|
|
NR_104242.2:n.784A=
|
|
|
NR_104243.2:n.722A=
|
|
|
NM_001282788.3:c.733A=
MANE Select
|
NP_001269717.1:p.Ile245=
|
|