ENST00000389857.11:c.5138C>T
MANE Select
|
ENSP00000374507.6:p.Pro1713Leu
|
|
ENST00000331194.8:c.710C>T
|
ENSP00000330332.8:p.Pro237Leu
|
|
ENST00000334448.5:n.950C>T
|
|
|
ENST00000389857.10:c.5138C>T
|
ENSP00000374507.6:p.Pro1713Leu
|
|
ENST00000556726.5:c.1366C>T
|
|
|
NM_001080414.3:c.5138C>T
|
NP_001073883.2:p.Pro1713Leu
|
|
XM_011536796.1:c.5030C>T
|
XP_011535098.1:p.Pro1677Leu
|
|
XR_429316.2:n.5413C>T
|
|
|
XM_011536796.2:c.5030C>T
|
XP_011535098.1:p.Pro1677Leu
|
|
XM_017021336.1:c.2219C>T
|
XP_016876825.1:p.Pro740Leu
|
|
XR_429316.4:n.5411C>T
|
|
|
NM_001080414.4:c.5138C>T
MANE Select
|
NP_001073883.2:p.Pro1713Leu
|
|