ENST00000216373.10:c.441T>G
MANE Select
|
ENSP00000216373.5:p.Asn147Lys
|
|
ENST00000216373.9:c.441T>G
|
ENSP00000216373.5:p.Asn147Lys
|
|
ENST00000543680.5:c.441T>G
|
ENSP00000445328.1:p.Asn147Lys
|
|
ENST00000555666.1:n.620T>G
|
|
|
ENST00000556469.5:n.412T>G
|
|
|
NM_006939.2:c.441T>G
|
NP_008870.2:p.Asn147Lys
|
|
XM_005268021.1:c.261T>G
|
XP_005268078.1:p.Asn87Lys
|
|
XM_011537103.1:c.402T>G
|
XP_011535405.1:p.Asn134Lys
|
|
XM_011537104.1:c.441T>G
|
XP_011535406.1:p.Asn147Lys
|
|
XR_943842.1:n.1039+15888A>C
|
|
|
XR_943843.1:n.1039+15888A>C
|
|
|
NM_006939.3:c.441T>G
|
NP_008870.2:p.Asn147Lys
|
|
NM_006939.4:c.441T>G
MANE Select
|
NP_008870.2:p.Asn147Lys
|
|