ENST00000389857.11:c.5197G>T
MANE Select
|
ENSP00000374507.6:p.Val1733Phe
|
|
ENST00000331194.8:c.769G>T
|
ENSP00000330332.8:p.Val257Phe
|
|
ENST00000334448.5:n.1009G>T
|
|
|
ENST00000389857.10:c.5197G>T
|
ENSP00000374507.6:p.Val1733Phe
|
|
ENST00000556726.5:c.1425G>T
|
|
|
NM_001080414.3:c.5197G>T
|
NP_001073883.2:p.Val1733Phe
|
|
XM_011536796.1:c.5089G>T
|
XP_011535098.1:p.Val1697Phe
|
|
XR_429316.2:n.5472G>T
|
|
|
XM_011536796.2:c.5089G>T
|
XP_011535098.1:p.Val1697Phe
|
|
XM_017021336.1:c.2278G>T
|
XP_016876825.1:p.Val760Phe
|
|
XR_429316.4:n.5470G>T
|
|
|
NM_001080414.4:c.5197G>T
MANE Select
|
NP_001073883.2:p.Val1733Phe
|
|