ENST00000379270.5:c.-37G>C
MANE Select
|
ENSP00000368572.4:n.-37G>C
|
|
ENST00000683890.1:c.38G>C
|
ENSP00000506989.1:p.Gly13Ala
|
|
ENST00000379251.7:c.-37G>C
|
ENSP00000368553.3:n.-37G>C
|
|
ENST00000379253.7:c.-37G>C
|
ENSP00000368555.3:n.-37G>C
|
|
ENST00000379254.5:c.-37G>C
|
ENSP00000368556.1:n.-37G>C
|
|
ENST00000379270.4:c.-37G>C
|
ENSP00000368572.4:n.-37G>C
|
|
ENST00000489394.5:n.119G>C
|
|
|
NM_002970.3:c.-37G>C
|
NP_002961.1:n.-37G>C
|
|
NR_027783.2:n.158G>C
|
|
|
XM_024452421.1:c.-1376G>C
|
XP_024308189.1:n.-1376G>C
|
|
NM_002970.4:c.-37G>C
MANE Select
|
NP_002961.1:n.-37G>C
|
|
NR_027783.3:n.143G>C
|
|
|