ENST00000389857.11:c.5121A>C
MANE Select
|
ENSP00000374507.6:p.Pro1707=
|
|
ENST00000331194.8:c.693A>C
|
ENSP00000330332.8:p.Pro231=
|
|
ENST00000334448.5:n.933A>C
|
|
|
ENST00000389857.10:c.5121A>C
|
ENSP00000374507.6:p.Pro1707=
|
|
ENST00000556726.5:c.1349A>C
|
|
|
NM_001080414.3:c.5121A>C
|
NP_001073883.2:p.Pro1707=
|
|
XM_011536796.1:c.5013A>C
|
XP_011535098.1:p.Pro1671=
|
|
XR_429316.2:n.5396A>C
|
|
|
XM_011536796.2:c.5013A>C
|
XP_011535098.1:p.Pro1671=
|
|
XM_017021336.1:c.2202A>C
|
XP_016876825.1:p.Pro734=
|
|
XR_429316.4:n.5394A>C
|
|
|
NM_001080414.4:c.5121A>C
MANE Select
|
NP_001073883.2:p.Pro1707=
|
|