ENST00000346342.8:c.1321G>C
MANE Select
|
ENSP00000329546.4:p.Ala441Pro
|
|
ENST00000346342.7:c.1321G>C
|
ENSP00000329546.3:p.Ala441Pro
|
|
ENST00000375581.3:c.1387G>C
|
ENSP00000364731.3:p.Ala463Pro
|
|
ENST00000541084.5:c.1135G>C
|
ENSP00000442051.2:p.Ala379Pro
|
|
NM_000131.4:c.1387G>C , LRG_554t1:c.1387G>C
|
NP_000122.1:p.Ala463Pro
|
|
NM_001267554.1:c.1135G>C
|
NP_001254483.1:p.Ala379Pro
|
|
NM_019616.3:c.1321G>C , LRG_554t2:c.1321G>C
|
NP_062562.1:p.Ala441Pro
|
|
NR_051961.1:n.1408G>C
|
|
|
XM_006719963.2:c.1180G>C
|
XP_006720026.1:p.Ala394Pro
|
|
XM_011537474.1:c.1429G>C
|
XP_011535776.1:p.Ala477Pro
|
|
XM_011537475.1:c.1243G>C
|
XP_011535777.1:p.Ala415Pro
|
|
XM_011537476.1:c.1081G>C
|
XP_011535778.1:p.Ala361Pro
|
|
XM_011537477.1:c.1390G>C
|
XP_011535779.1:p.Ala464Pro
|
|
XM_006719963.3:c.1225G>C
|
XP_006720026.2:p.Ala409Pro
|
|
XM_011537474.2:c.1474G>C
|
XP_011535776.2:p.Ala492Pro
|
|
XM_011537475.2:c.1288G>C
|
XP_011535777.2:p.Ala430Pro
|
|
XM_011537476.2:c.1081G>C
|
XP_011535778.1:p.Ala361Pro
|
|
NM_019616.4:c.1321G>C
MANE Select
|
NP_062562.1:p.Ala441Pro
|
|
NR_051961.2:n.1405G>C
|
|
|
NM_001267554.2:c.1135G>C
|
NP_001254483.1:p.Ala379Pro
|
|