ENST00000362072.8:c.955C>G
MANE Select
|
ENSP00000354859.3:p.Pro319Ala
|
|
ENST00000346454.7:c.868C>G
|
ENSP00000278597.5:p.Pro290Ala
|
|
ENST00000362072.7:c.955C>G
|
ENSP00000354859.3:p.Pro319Ala
|
|
ENST00000538967.5:c.961C>G
|
ENSP00000438215.1:p.Pro321Ala
|
|
ENST00000542968.5:c.955C>G
|
ENSP00000442172.1:p.Pro319Ala
|
|
ENST00000544518.5:c.952C>G
|
ENSP00000441068.1:p.Pro318Ala
|
|
NM_000795.3:c.955C>G
|
NP_000786.1:p.Pro319Ala
|
|
NM_016574.3:c.868C>G
|
NP_057658.2:p.Pro290Ala
|
|
XM_017017296.2:c.955C>G
|
XP_016872785.1:p.Pro319Ala
|
|
NM_000795.4:c.955C>G
MANE Select
|
NP_000786.1:p.Pro319Ala
|
|
NM_016574.4:c.868C>G
|
NP_057658.2:p.Pro290Ala
|
|