|
ENST00000234071.8:c.86G>T
MANE Select
|
ENSP00000234071.4:p.Ser29Ile
|
|
|
ENST00000234071.7:c.86G>T
|
ENSP00000234071.3:p.Ser29Ile
|
|
|
ENST00000409048.1:c.86G>T
|
ENSP00000386679.1:p.Ser29Ile
|
|
|
ENST00000419985.5:c.71-20G>T
|
ENSP00000392606.1:n.71-20G>T
|
|
|
ENST00000427769.5:c.86G>T
|
ENSP00000406295.1:p.Ser29Ile
|
|
|
ENST00000429925.5:c.86G>T
|
ENSP00000412697.1:p.Ser29Ile
|
|
|
ENST00000431364.1:c.71-20G>T
|
ENSP00000391220.1:n.71-20G>T
|
|
|
ENST00000442644.5:c.86G>T
|
ENSP00000411241.1:p.Ser29Ile
|
|
|
ENST00000474030.5:n.169G>T
|
|
|
|
NM_000312.3:c.86G>T , LRG_599t1:c.86G>T
|
NP_000303.1:p.Ser29Ile
|
|
|
XM_005263715.3:c.269G>T
|
XP_005263772.1:p.Ser90Ile
|
|
|
XM_005263716.3:c.149G>T
|
XP_005263773.1:p.Ser50Ile
|
|
|
XM_005263717.3:c.149G>T
|
XP_005263774.1:p.Ser50Ile
|
|
|
XM_005263717.4:c.149G>T
|
XP_005263774.1:p.Ser50Ile
|
|
|
XM_017004505.1:c.349-20G>T
|
XP_016859994.1:n.349-20G>T
|
|
|
XM_024453002.1:c.349-20G>T
|
XP_024308770.1:n.349-20G>T
|
|
|
XM_024453003.1:c.269G>T
|
XP_024308771.1:p.Ser90Ile
|
|
|
XM_024453004.1:c.269G>T
|
XP_024308772.1:p.Ser90Ile
|
|
|
XM_024453005.1:c.149G>T
|
XP_024308773.1:p.Ser50Ile
|
|
|
XM_024453006.1:c.86G>T
|
XP_024308774.1:p.Ser29Ile
|
|
|
NM_000312.4:c.86G>T
MANE Select
|
NP_000303.1:p.Ser29Ile
|
|
|
NM_001375602.1:c.269G>T
|
NP_001362531.1:p.Ser90Ile
|
|
|
NM_001375603.1:c.149G>T
|
NP_001362532.1:p.Ser50Ile
|
|
|
NM_001375604.1:c.149G>T
|
NP_001362533.1:p.Ser50Ile
|
|
|
NM_001375605.1:c.86G>T
|
NP_001362534.1:p.Ser29Ile
|
|
|
NM_001375606.1:c.149G>T
|
NP_001362535.1:p.Ser50Ile
|
|
|
NM_001375607.1:c.190-20G>T
|
NP_001362536.1:n.190-20G>T
|
|
|
NM_001375608.1:c.86G>T
|
NP_001362537.1:p.Ser29Ile
|
|
|
NM_001375609.1:c.62G>T
|
NP_001362538.1:p.Ser21Ile
|
|
|
NM_001375610.1:c.80G>T
|
NP_001362539.1:p.Ser27Ile
|
|
|
NM_001375611.1:c.86G>T
|
NP_001362540.1:p.Ser29Ile
|
|
|
NM_001375613.1:c.86G>T
|
NP_001362542.1:p.Ser29Ile
|
|
