ENST00000298910.12:c.5612A>C
MANE Select
|
ENSP00000298910.7:p.Asn1871Thr
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|
ENST00000679360.1:c.*4521A>C
|
ENSP00000505368.1:n.*4521A>C
|
|
ENST00000679532.1:c.1386A>C
|
|
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ENST00000680018.1:c.1057A>C
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ENSP00000505347.1:n.1057A>C
|
|
ENST00000680422.1:c.1257A>C
|
|
|
ENST00000680425.1:c.779A>C
|
ENSP00000506459.1:n.779A>C
|
|
ENST00000680453.1:c.1069A>C
|
|
|
ENST00000680790.1:c.5357A>C
|
ENSP00000505335.1:p.Asn1786Thr
|
|
ENST00000681136.1:n.1596A>C
|
|
|
ENST00000681696.1:c.1295A>C
|
ENSP00000505871.1:p.Asn432Thr
|
|
ENST00000298910.11:c.5612A>C
|
ENSP00000298910.7:p.Asn1871Thr
|
|
ENST00000430804.5:c.2908A>C
|
|
|
ENST00000479187.5:n.2293A>C
|
|
|
NM_198578.3:c.5612A>C
|
NP_940980.3:p.Asn1871Thr
|
|
XM_005268629.2:c.5612A>C
|
XP_005268686.1:p.Asn1871Thr
|
|
XM_011537877.1:c.5612A>C
|
XP_011536179.1:p.Asn1871Thr
|
|
XM_011537878.1:c.5612A>C
|
XP_011536180.1:p.Asn1871Thr
|
|
XM_011537879.1:c.4409A>C
|
XP_011536181.1:p.Asn1470Thr
|
|
XM_005268629.4:c.5612A>C
|
XP_005268686.1:p.Asn1871Thr
|
|
XM_011537877.3:c.5612A>C
|
XP_011536179.1:p.Asn1871Thr
|
|
XM_017018787.1:c.2528A>C
|
XP_016874276.1:p.Asn843Thr
|
|
XM_017018788.2:c.1874A>C
|
XP_016874277.1:p.Asn625Thr
|
|
XM_024448833.1:c.4409A>C
|
XP_024304601.1:p.Asn1470Thr
|
|
NM_198578.4:c.5612A>C
MANE Select
|
NP_940980.4:p.Asn1871Thr
|
|