ENST00000272895.12:c.4731C>G
MANE Select
|
ENSP00000272895.7:p.Thr1577=
|
|
ENST00000272895.11:c.4731C>G
|
ENSP00000272895.7:p.Thr1577=
|
|
ENST00000389661.4:c.3777C>G
|
ENSP00000374312.4:p.Thr1259=
|
|
NM_015657.3:c.3777C>G
|
NP_056472.2:p.Thr1259=
|
|
NM_173076.2:c.4731C>G
|
NP_775099.2:p.Thr1577=
|
|
NR_103740.1:n.5031C>G
|
|
|
XM_011510951.1:c.4740C>G
|
XP_011509253.1:p.Thr1580=
|
|
XM_011510952.1:c.4740C>G
|
XP_011509254.1:p.Thr1580=
|
|
XM_011510951.2:c.4740C>G
|
XP_011509253.1:p.Thr1580=
|
|
NM_173076.3:c.4731C>G
MANE Select
|
NP_775099.2:p.Thr1577=
|
|
NR_103740.2:n.5229C>G
|
|
|
NM_015657.4:c.3777C>G
|
NP_056472.2:p.Thr1259=
|
|