ENST00000622290.5:c.*600G>T
|
ENSP00000483331.2:n.*600G>T
|
|
ENST00000205557.12:c.4428G>T
MANE Select
|
ENSP00000205557.7:p.Gln1476His
|
|
ENST00000640696.1:c.1242G>T
|
ENSP00000492197.1:p.Gln414His
|
|
ENST00000205557.11:c.4428G>T
|
ENSP00000205557.7:p.Gln1476His
|
|
ENST00000456970.6:c.4053G>T
|
ENSP00000405002.2:n.4053G>T
|
|
ENST00000576204.5:n.1291G>T
|
|
|
ENST00000622290.4:c.*1637G>T
|
ENSP00000483331.1:n.*1637G>T
|
|
NM_001171.5:c.4428G>T
|
NP_001162.4:p.Gln1476His
|
|
XM_011522479.1:c.4395G>T
|
XP_011520781.1:p.Gln1465His
|
|
XM_011522480.1:c.4086G>T
|
XP_011520782.1:p.Gln1362His
|
|
XM_011522481.1:c.4086G>T
|
XP_011520783.1:p.Gln1362His
|
|
XR_933134.1:n.538+5927C>A
|
|
|
NM_001351800.1:c.4086G>T
|
NP_001338729.1:p.Gln1362His
|
|
NR_147784.1:n.4090G>T
|
|
|
XM_011522479.2:c.4395G>T
|
XP_011520781.1:p.Gln1465His
|
|
XM_011522481.3:c.4086G>T
|
XP_011520783.1:p.Gln1362His
|
|
XM_017023212.1:c.4260G>T
|
XP_016878701.1:p.Gln1420His
|
|
XM_024450261.1:c.4464G>T
|
XP_024306029.1:p.Gln1488His
|
|
NM_001171.6:c.4428G>T
MANE Select
|
NP_001162.5:p.Gln1476His
|
|