|
NM_138694.4:c.2936C>T
MANE Select
|
NP_619639.3:p.Thr979Ile
|
|
ENST00000371117.8:c.2936C>T
MANE Select
|
ENSP00000360158.3:p.Thr979Ile
|
|
NM_138694.3:c.2936C>T
|
NP_619639.3:p.Thr979Ile
|
|
NM_170724.2:c.2936C>T
|
NP_733842.2:p.Thr979Ile
|
|
NM_170724.3:c.2936C>T
|
NP_733842.2:p.Thr979Ile
|
|
ENST00000340994.4:c.2936C>T
|
ENSP00000341097.4:p.Thr979Ile
|
|
ENST00000371117.7:c.2936C>T
|
ENSP00000360158.3:p.Thr979Ile
|
|
XM_011514679.1:c.2936C>T
|
XP_011512981.1:p.Thr979Ile
|
|
XM_011514680.1:c.2936C>T
|
XP_011512982.1:p.Thr979Ile
|
|
XM_011514680.3:c.2936C>T
|
XP_011512982.1:p.Thr979Ile
|
|
XM_011514681.1:c.2936C>T
|
XP_011512983.1:p.Thr979Ile
|
|
XM_011514682.1:c.2936C>T
|
XP_011512984.1:p.Thr979Ile
|
|
XM_011514682.3:c.2936C>T
|
XP_011512984.1:p.Thr979Ile
|
|
XM_011514683.1:c.2936C>T
|
XP_011512985.1:p.Thr979Ile
|
|
XM_011514683.3:c.2936C>T
|
XP_011512985.1:p.Thr979Ile
|
|
XM_011514684.1:c.2225C>T
|
XP_011512986.1:p.Thr742Ile
|
|
XM_011514684.3:c.2225C>T
|
XP_011512986.1:p.Thr742Ile
|
|
XM_011514685.1:c.2936C>T
|
XP_011512987.1:p.Thr979Ile
|
|
XM_011514686.1:c.2936C>T
|
XP_011512988.1:p.Thr979Ile
|
|
XM_011514686.2:c.2936C>T
|
XP_011512988.1:p.Thr979Ile
|
|
XM_011514687.1:c.2936C>T
|
XP_011512989.1:p.Thr979Ile
|
|
XM_011514688.1:c.2936C>T
|
XP_011512990.1:p.Thr979Ile
|
|
XM_011514688.2:c.2936C>T
|
XP_011512990.1:p.Thr979Ile
|
|
XM_011514689.1:c.2936C>T
|
XP_011512991.1:p.Thr979Ile
|
|
XM_017010944.2:c.2936C>T
|
XP_016866433.1:p.Thr979Ile
|
|
XM_017010945.2:c.2861C>T
|
XP_016866434.1:p.Thr954Ile
|
|
XM_017010946.2:c.2936C>T
|
XP_016866435.1:p.Thr979Ile
|
|
XM_017010947.2:c.2936C>T
|
XP_016866436.1:p.Thr979Ile
|
|
XM_017010948.2:c.2225C>T
|
XP_016866437.1:p.Thr742Ile
|
|
XM_017010949.2:c.1076C>T
|
XP_016866438.1:p.Thr359Ile
|
|
XM_017010950.1:c.2936C>T
|
XP_016866439.1:p.Thr979Ile
|
|
XM_017010951.1:c.2936C>T
|
XP_016866440.1:p.Thr979Ile
|
|
XM_017010952.1:c.2936C>T
|
XP_016866441.1:p.Thr979Ile
|
|
XR_001743469.1:n.3212C>T
|
|
