ENST00000298910.12:c.7057A>C
MANE Select
|
ENSP00000298910.7:p.Asn2353His
|
|
ENST00000636518.1:c.854A>C
|
|
|
ENST00000679360.1:c.*5966A>C
|
ENSP00000505368.1:n.*5966A>C
|
|
ENST00000679532.1:c.2831A>C
|
|
|
ENST00000679683.1:c.847A>C
|
|
|
ENST00000680018.1:c.2502A>C
|
ENSP00000505347.1:n.2502A>C
|
|
ENST00000680422.1:c.4144A>C
|
|
|
ENST00000680425.1:c.2224A>C
|
ENSP00000506459.1:n.2224A>C
|
|
ENST00000680453.1:c.2514A>C
|
|
|
ENST00000680790.1:c.6802A>C
|
ENSP00000505335.1:p.Asn2268His
|
|
ENST00000681136.1:n.3041A>C
|
|
|
ENST00000681696.1:c.2740A>C
|
ENSP00000505871.1:p.Asn914His
|
|
ENST00000681773.1:n.264A>C
|
|
|
ENST00000298910.11:c.7057A>C
|
ENSP00000298910.7:p.Asn2353His
|
|
ENST00000430804.5:c.4353A>C
|
|
|
ENST00000479187.5:n.3738A>C
|
|
|
NM_198578.3:c.7057A>C
|
NP_940980.3:p.Asn2353His
|
|
XM_005268629.2:c.7057A>C
|
XP_005268686.1:p.Asn2353His
|
|
XM_011537877.1:c.7057A>C
|
XP_011536179.1:p.Asn2353His
|
|
XM_011537879.1:c.5854A>C
|
XP_011536181.1:p.Asn1952His
|
|
XR_944868.1:n.485-8603T>G
|
|
|
XM_005268629.4:c.7057A>C
|
XP_005268686.1:p.Asn2353His
|
|
XM_011537877.3:c.7057A>C
|
XP_011536179.1:p.Asn2353His
|
|
XM_017018787.1:c.3973A>C
|
XP_016874276.1:p.Asn1325His
|
|
XM_017018788.2:c.3319A>C
|
XP_016874277.1:p.Asn1107His
|
|
XM_024448833.1:c.5854A>C
|
XP_024304601.1:p.Asn1952His
|
|
XR_944868.2:n.485-8603T>G
|
|
|
NM_198578.4:c.7057A>C
MANE Select
|
NP_940980.4:p.Asn2353His
|
|