ENST00000367698.4:c.1150C>T
MANE Select
|
ENSP00000356671.3:p.Pro384Ser
|
|
ENST00000367698.3:c.1150C>T
|
ENSP00000356671.3:p.Pro384Ser
|
|
ENST00000617423.4:c.560-2062C>T
|
ENSP00000478688.1:n.560-2062C>T
|
|
NM_000488.3:c.1150C>T , LRG_577t1:c.1150C>T
|
NP_000479.1:p.Pro384Ser
|
|
XM_005245198.2:c.1006C>T
|
XP_005245255.1:p.Pro336Ser
|
|
NM_001365052.1:c.1006C>T
|
NP_001351981.1:p.Pro336Ser
|
|
NM_000488.4:c.1150C>T
MANE Select
|
NP_000479.1:p.Pro384Ser
|
|
NM_001365052.2:c.1006C>T
|
NP_001351981.1:p.Pro336Ser
|
|
NM_001386302.1:c.1273C>T
|
NP_001373231.1:p.Pro425Ser
|
|
NM_001386303.1:c.1231C>T
|
NP_001373232.1:p.Pro411Ser
|
|
NM_001386304.1:c.1129C>T
|
NP_001373233.1:p.Pro377Ser
|
|
NM_001386305.1:c.1093C>T
|
NP_001373234.1:p.Pro365Ser
|
|
NM_001386306.1:c.934C>T
|
NP_001373235.1:p.Pro312Ser
|
|