ENST00000318158.11:c.129G>C
MANE Select
|
ENSP00000313432.6:p.Lys43Asn
|
|
ENST00000318158.10:c.129G>C
|
ENSP00000313432.6:p.Lys43Asn
|
|
ENST00000377824.8:n.166G>C
|
|
|
ENST00000460882.5:n.156G>C
|
|
|
ENST00000487399.5:n.138G>C
|
|
|
ENST00000491488.5:n.109+2057G>C
|
|
|
ENST00000493368.5:n.186G>C
|
|
|
ENST00000607784.1:c.129G>C
|
ENSP00000475569.1:p.Lys43Asn
|
|
NM_012203.1:c.129G>C
|
NP_036335.1:p.Lys43Asn
|
|
XM_005251631.1:c.83+2057G>C
|
XP_005251688.1:n.83+2057G>C
|
|
XM_011518073.1:c.-634G>C
|
XP_011516375.1:n.-634G>C
|
|
XR_929374.1:n.214G>C
|
|
|
XM_017015320.2:c.129G>C
|
XP_016870809.1:p.Lys43Asn
|
|
XM_017015321.2:c.129G>C
|
XP_016870810.1:p.Lys43Asn
|
|
XM_017015323.2:c.-634G>C
|
XP_016870812.1:n.-634G>C
|
|
XM_024447716.1:c.402G>C
|
XP_024303484.1:p.Lys134Asn
|
|
XM_024447717.1:c.402G>C
|
XP_024303485.1:p.Lys134Asn
|
|
XR_002956828.1:n.417G>C
|
|
|
XR_002956829.1:n.417G>C
|
|
|
XR_002956830.1:n.188G>C
|
|
|
XR_002956831.1:n.138+2057G>C
|
|
|
XR_002956832.1:n.188G>C
|
|
|
NM_012203.2:c.129G>C
MANE Select
|
NP_036335.1:p.Lys43Asn
|
|