|
NM_000540.3:c.14864T>C
MANE Select
|
NP_000531.2:p.Met4955Thr
|
|
ENST00000359596.8:c.14864T>C
MANE Select
|
ENSP00000352608.2:p.Met4955Thr
|
|
NM_000540.2:c.14864T>C , LRG_766t1:c.14864T>C
|
NP_000531.2:p.Met4955Thr
|
|
NM_001042723.1:c.14849T>C
|
NP_001036188.1:p.Met4950Thr
|
|
NM_001042723.2:c.14849T>C
|
NP_001036188.1:p.Met4950Thr
|
|
ENST00000355481.8:c.14849T>C
|
ENSP00000347667.3:p.Met4950Thr
|
|
ENST00000359596.7:c.14864T>C
|
ENSP00000352608.2:p.Met4955Thr
|
|
ENST00000360985.7:c.14846T>C
|
ENSP00000354254.4:p.Met4949Thr
|
|
ENST00000593677.2:c.1800T>C
|
|
|
ENST00000688602.1:c.3197T>C
|
|
|
ENST00000689936.1:c.3169T>C
|
|
|
ENST00000692547.1:n.257T>C
|
|
|
XM_006723317.1:c.14846T>C
|
XP_006723380.1:p.Met4949Thr
|
|
XM_006723317.2:c.14846T>C
|
XP_006723380.1:p.Met4949Thr
|
|
XM_006723319.1:c.14831T>C
|
XP_006723382.1:p.Met4944Thr
|
|
XM_006723319.2:c.14831T>C
|
XP_006723382.1:p.Met4944Thr
|
|
XM_011527204.1:c.14861T>C
|
XP_011525506.1:p.Met4954Thr
|
|
XM_011527205.1:c.14777T>C
|
XP_011525507.1:p.Met4926Thr
|
|
XM_011527205.2:c.14777T>C
|
XP_011525507.1:p.Met4926Thr
|
