ENST00000367698.4:c.1274G>C
MANE Select
|
ENSP00000356671.3:p.Arg425Pro
|
|
ENST00000367698.3:c.1274G>C
|
ENSP00000356671.3:p.Arg425Pro
|
|
ENST00000617423.4:c.659G>C
|
ENSP00000478688.1:p.Arg220Pro
|
|
NM_000488.3:c.1274G>C , LRG_577t1:c.1274G>C
|
NP_000479.1:p.Arg425Pro
|
|
XM_005245198.2:c.1130G>C
|
XP_005245255.1:p.Arg377Pro
|
|
NM_001365052.1:c.1130G>C
|
NP_001351981.1:p.Arg377Pro
|
|
NM_000488.4:c.1274G>C
MANE Select
|
NP_000479.1:p.Arg425Pro
|
|
NM_001365052.2:c.1130G>C
|
NP_001351981.1:p.Arg377Pro
|
|
NM_001386302.1:c.1397G>C
|
NP_001373231.1:p.Arg466Pro
|
|
NM_001386303.1:c.1355G>C
|
NP_001373232.1:p.Arg452Pro
|
|
NM_001386304.1:c.1253G>C
|
NP_001373233.1:p.Arg418Pro
|
|
NM_001386305.1:c.1217G>C
|
NP_001373234.1:p.Arg406Pro
|
|
NM_001386306.1:c.1058G>C
|
NP_001373235.1:p.Arg353Pro
|
|