ENST00000389857.11:c.5175C>A
MANE Select
|
ENSP00000374507.6:p.Pro1725=
|
|
ENST00000331194.8:c.747C>A
|
ENSP00000330332.8:p.Pro249=
|
|
ENST00000334448.5:n.987C>A
|
|
|
ENST00000389857.10:c.5175C>A
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ENSP00000374507.6:p.Pro1725=
|
|
ENST00000556726.5:c.1403C>A
|
|
|
NM_001080414.3:c.5175C>A
|
NP_001073883.2:p.Pro1725=
|
|
XM_011536796.1:c.5067C>A
|
XP_011535098.1:p.Pro1689=
|
|
XR_429316.2:n.5450C>A
|
|
|
XM_011536796.2:c.5067C>A
|
XP_011535098.1:p.Pro1689=
|
|
XM_017021336.1:c.2256C>A
|
XP_016876825.1:p.Pro752=
|
|
XR_429316.4:n.5448C>A
|
|
|
NM_001080414.4:c.5175C>A
MANE Select
|
NP_001073883.2:p.Pro1725=
|
|