ENST00000278935.8:c.1853T>C
MANE Select
|
ENSP00000278935.3:p.Met618Thr
|
|
ENST00000278935.7:c.1853T>C
|
ENSP00000278935.3:p.Met618Thr
|
|
ENST00000529153.5:n.302T>C
|
|
|
ENST00000533223.1:n.2735T>C
|
|
|
ENST00000533675.5:n.1961T>C
|
|
|
ENST00000533706.5:n.1177T>C
|
|
|
NM_001271933.1:c.1862T>C
|
NP_001258862.1:p.Met621Thr
|
|
NM_014956.4:c.1853T>C
|
NP_055771.4:p.Met618Thr
|
|
XM_005271453.1:c.3539T>C
|
XP_005271510.1:p.Met1180Thr
|
|
XM_005271456.1:c.1853T>C
|
XP_005271513.1:p.Met618Thr
|
|
XM_005271457.1:c.1862T>C
|
XP_005271514.1:p.Met621Thr
|
|
XM_006718788.1:c.3548T>C
|
XP_006718851.1:p.Met1183Thr
|
|
XM_006718794.1:c.1775T>C
|
XP_006718857.1:p.Met592Thr
|
|
XM_011542670.1:c.3608T>C
|
XP_011540972.1:p.Met1203Thr
|
|
XM_011542671.1:c.3608T>C
|
XP_011540973.1:p.Met1203Thr
|
|
XM_011542672.1:c.3608T>C
|
XP_011540974.1:p.Met1203Thr
|
|
XM_011542673.1:c.3608T>C
|
XP_011540975.1:p.Met1203Thr
|
|
XM_011542674.1:c.3599T>C
|
XP_011540976.1:p.Met1200Thr
|
|
XM_011542675.1:c.3608T>C
|
XP_011540977.1:p.Met1203Thr
|
|
XM_011542676.1:c.3530T>C
|
XP_011540978.1:p.Met1177Thr
|
|
XM_011542677.1:c.3470T>C
|
XP_011540979.1:p.Met1157Thr
|
|
XM_011542678.1:c.3470T>C
|
XP_011540980.1:p.Met1157Thr
|
|
XM_011542679.1:c.3461T>C
|
XP_011540981.1:p.Met1154Thr
|
|
XM_011542680.1:c.3362T>C
|
XP_011540982.1:p.Met1121Thr
|
|
XM_011542681.1:c.3333-3446T>C
|
XP_011540983.1:n.3333-3446T>C
|
|
XM_011542682.1:c.1922T>C
|
XP_011540984.1:p.Met641Thr
|
|
XM_011542683.1:c.1922T>C
|
XP_011540985.1:p.Met641Thr
|
|
XM_011542685.1:c.1844T>C
|
XP_011540987.1:p.Met615Thr
|
|
XM_011542686.1:c.1844T>C
|
XP_011540988.1:p.Met615Thr
|
|
XM_011542687.1:c.1784T>C
|
XP_011540989.1:p.Met595Thr
|
|
XM_011542688.1:c.1583T>C
|
XP_011540990.1:p.Met528Thr
|
|
XR_428971.2:n.3819T>C
|
|
|
XR_947808.1:n.4026T>C
|
|
|
XR_947809.1:n.4026T>C
|
|
|
XR_947810.1:n.3957T>C
|
|
|
XR_947811.1:n.4162T>C
|
|
|
XM_017017364.1:c.3599T>C
|
XP_016872853.1:p.Met1200Thr
|
|
XM_017017365.1:c.3599T>C
|
XP_016872854.1:p.Met1200Thr
|
|
XM_017017366.1:c.3599T>C
|
XP_016872855.1:p.Met1200Thr
|
|
XM_017017367.1:c.3599T>C
|
XP_016872856.1:p.Met1200Thr
|
|
XM_017017368.1:c.3599T>C
|
XP_016872857.1:p.Met1200Thr
|
|
XM_017017369.1:c.3599T>C
|
XP_016872858.1:p.Met1200Thr
|
|
XM_017017370.1:c.3599T>C
|
XP_016872859.1:p.Met1200Thr
|
|
XM_017017371.1:c.3521T>C
|
XP_016872860.1:p.Met1174Thr
|
|
XM_017017372.1:c.3461T>C
|
XP_016872861.1:p.Met1154Thr
|
|
XM_017017373.2:c.3461T>C
|
XP_016872862.1:p.Met1154Thr
|
|
XM_017017374.1:c.3461T>C
|
XP_016872863.1:p.Met1154Thr
|
|
XM_017017375.2:c.3461T>C
|
XP_016872864.1:p.Met1154Thr
|
|
XM_017017376.1:c.3452T>C
|
XP_016872865.1:p.Met1151Thr
|
|
XM_017017377.2:c.3353T>C
|
XP_016872866.1:p.Met1118Thr
|
|
XM_017017378.1:c.3324-3446T>C
|
XP_016872867.1:n.3324-3446T>C
|
|
XM_017017379.1:c.1913T>C
|
XP_016872868.1:p.Met638Thr
|
|
XM_017017380.1:c.1913T>C
|
XP_016872869.1:p.Met638Thr
|
|
XM_017017381.1:c.1835T>C
|
XP_016872870.1:p.Met612Thr
|
|
XM_017017382.1:c.1835T>C
|
XP_016872871.1:p.Met612Thr
|
|
XM_017017383.1:c.1775T>C
|
XP_016872872.1:p.Met592Thr
|
|
XM_017017384.1:c.1775T>C
|
XP_016872873.1:p.Met592Thr
|
|
XM_017017385.1:c.1574T>C
|
XP_016872874.1:p.Met525Thr
|
|
XM_017017386.1:c.1490T>C
|
XP_016872875.1:p.Met497Thr
|
|
XR_001747793.1:n.4017T>C
|
|
|
XR_001747794.1:n.4017T>C
|
|
|
XR_002957132.1:n.4017T>C
|
|
|
XR_002957133.1:n.3957T>C
|
|
|
XR_428971.3:n.3819T>C
|
|
|
NM_014956.5:c.1853T>C
MANE Select
|
NP_055771.4:p.Met618Thr
|
|
NM_001271933.2:c.1862T>C
|
NP_001258862.1:p.Met621Thr
|
|