ENST00000234071.8:c.570G>T
MANE Select
|
ENSP00000234071.4:p.Met190Ile
|
|
ENST00000234071.7:c.570G>T
|
ENSP00000234071.3:p.Met190Ile
|
|
ENST00000402125.2:c.121-2238G>T
|
|
|
ENST00000409048.1:c.672G>T
|
ENSP00000386679.1:p.Met224Ile
|
|
ENST00000442644.5:c.513G>T
|
ENSP00000411241.1:p.Met171Ile
|
|
ENST00000464089.1:n.156G>T
|
|
|
NM_000312.3:c.570G>T , LRG_599t1:c.570G>T
|
NP_000303.1:p.Met190Ile
|
|
XM_005263715.3:c.753G>T
|
XP_005263772.1:p.Met251Ile
|
|
XM_005263716.3:c.735G>T
|
XP_005263773.1:p.Met245Ile
|
|
XM_005263717.3:c.633G>T
|
XP_005263774.1:p.Met211Ile
|
|
XM_005263717.4:c.633G>T
|
XP_005263774.1:p.Met211Ile
|
|
XM_017004505.1:c.813G>T
|
XP_016859994.1:p.Met271Ile
|
|
XM_024453002.1:c.915G>T
|
XP_024308770.1:p.Met305Ile
|
|
XM_024453003.1:c.855G>T
|
XP_024308771.1:p.Met285Ile
|
|
XM_024453004.1:c.753G>T
|
XP_024308772.1:p.Met251Ile
|
|
XM_024453005.1:c.735G>T
|
XP_024308773.1:p.Met245Ile
|
|
XM_024453006.1:c.672G>T
|
XP_024308774.1:p.Met224Ile
|
|
XR_923313.2:n.4466C>A
|
|
|
NM_000312.4:c.570G>T
MANE Select
|
NP_000303.1:p.Met190Ile
|
|
NM_001375602.1:c.753G>T
|
NP_001362531.1:p.Met251Ile
|
|
NM_001375603.1:c.735G>T
|
NP_001362532.1:p.Met245Ile
|
|
NM_001375604.1:c.633G>T
|
NP_001362533.1:p.Met211Ile
|
|
NM_001375605.1:c.672G>T
|
NP_001362534.1:p.Met224Ile
|
|
NM_001375606.1:c.738G>T
|
NP_001362535.1:p.Met246Ile
|
|
NM_001375607.1:c.756G>T
|
NP_001362536.1:p.Met252Ile
|
|
NM_001375608.1:c.513G>T
|
NP_001362537.1:p.Met171Ile
|
|
NM_001375609.1:c.546G>T
|
NP_001362538.1:p.Met182Ile
|
|
NM_001375610.1:c.564G>T
|
NP_001362539.1:p.Met188Ile
|
|
NM_001375611.1:c.570G>T
|
NP_001362540.1:p.Met190Ile
|
|
NM_001375613.1:c.570G>T
|
NP_001362542.1:p.Met190Ile
|
|