ENST00000367698.4:c.1317T>C
MANE Select
|
ENSP00000356671.3:p.Pro439=
|
|
ENST00000367698.3:c.1317T>C
|
ENSP00000356671.3:p.Pro439=
|
|
ENST00000617423.4:c.702T>C
|
ENSP00000478688.1:p.Pro234=
|
|
NM_000488.3:c.1317T>C , LRG_577t1:c.1317T>C
|
NP_000479.1:p.Pro439=
|
|
XM_005245198.2:c.1173T>C
|
XP_005245255.1:p.Pro391=
|
|
NM_001365052.1:c.1173T>C
|
NP_001351981.1:p.Pro391=
|
|
NM_000488.4:c.1317T>C
MANE Select
|
NP_000479.1:p.Pro439=
|
|
NM_001365052.2:c.1173T>C
|
NP_001351981.1:p.Pro391=
|
|
NM_001386302.1:c.1440T>C
|
NP_001373231.1:p.Pro480=
|
|
NM_001386303.1:c.1398T>C
|
NP_001373232.1:p.Pro466=
|
|
NM_001386304.1:c.1296T>C
|
NP_001373233.1:p.Pro432=
|
|
NM_001386305.1:c.1260T>C
|
NP_001373234.1:p.Pro420=
|
|
NM_001386306.1:c.1101T>C
|
NP_001373235.1:p.Pro367=
|
|