ENST00000379270.5:c.3G>T
MANE Select
|
ENSP00000368572.4:p.Met1Ile
|
|
ENST00000683890.1:c.77G>T
|
ENSP00000506989.1:p.Trp26Leu
|
|
ENST00000379251.7:c.3G>T
|
ENSP00000368553.3:p.Met1Ile
|
|
ENST00000379253.7:c.3G>T
|
ENSP00000368555.3:p.Met1Ile
|
|
ENST00000379254.5:c.3G>T
|
ENSP00000368556.1:p.Met1Ile
|
|
ENST00000379270.4:c.3G>T
|
ENSP00000368572.4:p.Met1Ile
|
|
ENST00000463236.5:n.18G>T
|
|
|
ENST00000489394.5:n.158G>T
|
|
|
NM_002970.3:c.3G>T
|
NP_002961.1:p.Met1Ile
|
|
NR_027783.2:n.197G>T
|
|
|
XM_024452421.1:c.-1337G>T
|
XP_024308189.1:n.-1337G>T
|
|
NM_002970.4:c.3G>T
MANE Select
|
NP_002961.1:p.Met1Ile
|
|
NR_027783.3:n.182G>T
|
|
|