ENST00000348729.8:c.786G>C
MANE Select
|
ENSP00000302701.4:p.Met262Ile
|
|
ENST00000348729.7:c.786G>C
|
ENSP00000302701.4:p.Met262Ile
|
|
ENST00000353963.7:c.798G>C
|
ENSP00000302851.5:p.Met266Ile
|
|
ENST00000504513.1:c.164+139G>C
|
|
|
ENST00000506512.1:n.397G>C
|
|
|
NM_005847.4:c.786G>C
|
NP_005838.3:p.Met262Ile
|
|
NM_152685.3:c.798G>C
|
NP_689898.2:p.Met266Ile
|
|
XM_005272148.3:c.906G>C
|
XP_005272205.3:p.Met302Ile
|
|
XM_005272149.3:c.894G>C
|
XP_005272206.3:p.Met298Ile
|
|
XM_006714741.2:c.906G>C
|
XP_006714804.2:p.Met302Ile
|
|
XM_011543765.1:c.906G>C
|
XP_011542067.1:p.Met302Ile
|
|
XM_011543766.1:c.687G>C
|
XP_011542068.1:p.Met229Ile
|
|
XM_011543767.1:c.591G>C
|
XP_011542069.1:p.Met197Ile
|
|
XM_011543768.1:c.471G>C
|
XP_011542070.1:p.Met157Ile
|
|
XM_011543769.1:c.81G>C
|
XP_011542071.1:p.Met27Ile
|
|
XM_005272149.4:c.894G>C
|
XP_005272206.3:p.Met298Ile
|
|
XM_011543765.2:c.906G>C
|
XP_011542067.1:p.Met302Ile
|
|
NM_005847.5:c.786G>C
MANE Select
|
NP_005838.3:p.Met262Ile
|
|
NM_152685.4:c.798G>C
|
NP_689898.2:p.Met266Ile
|
|