ENST00000674895.3:c.867T>C
MANE Select
|
ENSP00000502087.2:p.Val289=
|
|
ENST00000674895.2:c.426T>C
|
ENSP00000502087.1:p.Val142=
|
|
ENST00000675057.1:c.426T>C
|
ENSP00000501832.1:p.Val142=
|
|
ENST00000675307.1:c.426T>C
|
ENSP00000501750.1:p.Val142=
|
|
ENST00000336648.8:c.426T>C
|
ENSP00000338387.3:p.Val142=
|
|
ENST00000399120.5:c.426T>C
|
ENSP00000382071.1:p.Val142=
|
|
ENST00000612277.4:c.426T>C
|
ENSP00000479939.1:p.Val142=
|
|
NM_000411.6:c.426T>C
|
NP_000402.3:p.Val142=
|
|
NM_001242784.1:c.426T>C
|
NP_001229713.1:p.Val142=
|
|
NM_001242785.1:c.426T>C
|
NP_001229714.1:p.Val142=
|
|
XM_005260953.2:c.867T>C
|
XP_005261010.1:p.Val289=
|
|
XM_005260954.1:c.867T>C
|
XP_005261011.1:p.Val289=
|
|
XM_005260955.2:c.426T>C
|
XP_005261012.1:p.Val142=
|
|
XM_005260956.2:c.426T>C
|
XP_005261013.1:p.Val142=
|
|
XM_006723994.1:c.426T>C
|
XP_006724057.1:p.Val142=
|
|
XM_006723995.1:c.426T>C
|
XP_006724058.1:p.Val142=
|
|
XM_011529538.1:c.426T>C
|
XP_011527840.1:p.Val142=
|
|
XM_011529539.1:c.426T>C
|
XP_011527841.1:p.Val142=
|
|
XM_011529540.1:c.867T>C
|
XP_011527842.1:p.Val289=
|
|
XM_011529541.1:c.426T>C
|
XP_011527843.1:p.Val142=
|
|
XM_011529542.1:c.867T>C
|
XP_011527844.1:p.Val289=
|
|
NM_000411.7:c.426T>C
|
NP_000402.3:p.Val142=
|
|
NM_001242784.2:c.426T>C
|
NP_001229713.1:p.Val142=
|
|
NM_001242785.2:c.426T>C
|
NP_001229714.1:p.Val142=
|
|
NM_001352514.1:c.867T>C
|
NP_001339443.1:p.Val289=
|
|
NM_001352515.1:c.426T>C
|
NP_001339444.1:p.Val142=
|
|
NM_001352516.1:c.426T>C
|
NP_001339445.1:p.Val142=
|
|
NM_001352517.1:c.426T>C
|
NP_001339446.1:p.Val142=
|
|
NM_001352518.1:c.426T>C
|
NP_001339447.1:p.Val142=
|
|
NR_148020.1:n.909T>C
|
|
|
NR_148021.1:n.883T>C
|
|
|
XM_011529539.3:c.426T>C
|
XP_011527841.1:p.Val142=
|
|
XM_011529540.2:c.867T>C
|
XP_011527842.1:p.Val289=
|
|
XM_017028330.1:c.426T>C
|
XP_016883819.1:p.Val142=
|
|
XM_024452065.1:c.255T>C
|
XP_024307833.1:p.Val85=
|
|
XM_024452066.1:c.255T>C
|
XP_024307834.1:p.Val85=
|
|
XR_001754835.1:n.868T>C
|
|
|
XR_001754836.1:n.868T>C
|
|
|
XR_001754837.2:n.868T>C
|
|
|
XR_001754840.1:n.868T>C
|
|
|
NM_000411.8:c.426T>C
|
NP_000402.3:p.Val142=
|
|
NM_001242784.3:c.426T>C
|
NP_001229713.1:p.Val142=
|
|
NM_001352514.2:c.867T>C
MANE Select
|
NP_001339443.1:p.Val289=
|
|
NM_001352515.2:c.426T>C
|
NP_001339444.1:p.Val142=
|
|
NM_001352516.2:c.426T>C
|
NP_001339445.1:p.Val142=
|
|
NR_148020.2:n.726T>C
|
|
|
NM_001352518.2:c.426T>C
|
NP_001339447.1:p.Val142=
|
|