ENST00000382844.2:c.111_114delinsTGTG
|
ENSP00000372295.1:p.Val37=
|
|
ENST00000382848.5:c.111_114delinsTGTG
MANE Select
|
ENSP00000372299.4:p.Val37=
|
|
ENST00000382844.1:c.111_114delinsTGTG
|
ENSP00000372295.1:p.Val37=
|
|
ENST00000382848.4:c.111_114delinsTGTG
|
ENSP00000372299.4:p.Val37=
|
|
NM_004004.5:c.111_114delinsTGTG
|
NP_003995.2:p.Val37=
|
|
XM_011535049.1:c.111_114delinsTGTG
|
XP_011533351.1:p.Val37=
|
|
XM_011535049.2:c.111_114delinsTGTG
|
XP_011533351.1:p.Val37=
|
|
NM_004004.6:c.111_114delinsTGTG
MANE Select
|
NP_003995.2:p.Val37=
|
|