ENST00000298910.12:c.5614A>T
MANE Select
|
ENSP00000298910.7:p.Asn1872Tyr
|
|
ENST00000679360.1:c.*4523A>T
|
ENSP00000505368.1:n.*4523A>T
|
|
ENST00000679532.1:c.1388A>T
|
|
|
ENST00000680018.1:c.1059A>T
|
ENSP00000505347.1:n.1059A>T
|
|
ENST00000680422.1:c.1259A>T
|
|
|
ENST00000680425.1:c.781A>T
|
ENSP00000506459.1:n.781A>T
|
|
ENST00000680453.1:c.1071A>T
|
|
|
ENST00000680790.1:c.5359A>T
|
ENSP00000505335.1:p.Asn1787Tyr
|
|
ENST00000681136.1:n.1598A>T
|
|
|
ENST00000681696.1:c.1297A>T
|
ENSP00000505871.1:p.Asn433Tyr
|
|
ENST00000298910.11:c.5614A>T
|
ENSP00000298910.7:p.Asn1872Tyr
|
|
ENST00000430804.5:c.2910A>T
|
|
|
ENST00000479187.5:n.2295A>T
|
|
|
NM_198578.3:c.5614A>T
|
NP_940980.3:p.Asn1872Tyr
|
|
XM_005268629.2:c.5614A>T
|
XP_005268686.1:p.Asn1872Tyr
|
|
XM_011537877.1:c.5614A>T
|
XP_011536179.1:p.Asn1872Tyr
|
|
XM_011537878.1:c.5614A>T
|
XP_011536180.1:p.Asn1872Tyr
|
|
XM_011537879.1:c.4411A>T
|
XP_011536181.1:p.Asn1471Tyr
|
|
XM_005268629.4:c.5614A>T
|
XP_005268686.1:p.Asn1872Tyr
|
|
XM_011537877.3:c.5614A>T
|
XP_011536179.1:p.Asn1872Tyr
|
|
XM_017018787.1:c.2530A>T
|
XP_016874276.1:p.Asn844Tyr
|
|
XM_017018788.2:c.1876A>T
|
XP_016874277.1:p.Asn626Tyr
|
|
XM_024448833.1:c.4411A>T
|
XP_024304601.1:p.Asn1471Tyr
|
|
NM_198578.4:c.5614A>T
MANE Select
|
NP_940980.4:p.Asn1872Tyr
|
|