ENST00000362072.8:c.1250T>C
MANE Select
|
ENSP00000354859.3:p.Val417Ala
|
|
ENST00000346454.7:c.1163T>C
|
ENSP00000278597.5:p.Val388Ala
|
|
ENST00000362072.7:c.1250T>C
|
ENSP00000354859.3:p.Val417Ala
|
|
ENST00000538967.5:c.1256T>C
|
ENSP00000438215.1:p.Val419Ala
|
|
ENST00000542968.5:c.1250T>C
|
ENSP00000442172.1:p.Val417Ala
|
|
ENST00000544518.5:c.1247T>C
|
ENSP00000441068.1:p.Val416Ala
|
|
NM_000795.3:c.1250T>C
|
NP_000786.1:p.Val417Ala
|
|
NM_016574.3:c.1163T>C
|
NP_057658.2:p.Val388Ala
|
|
XM_017017296.2:c.1250T>C
|
XP_016872785.1:p.Val417Ala
|
|
NM_000795.4:c.1250T>C
MANE Select
|
NP_000786.1:p.Val417Ala
|
|
NM_016574.4:c.1163T>C
|
NP_057658.2:p.Val388Ala
|
|