ENST00000298229.7:c.883C>T
MANE Select
|
ENSP00000298229.2:p.Pro295Ser
|
|
ENST00000298229.6:c.883C>T
|
ENSP00000298229.2:p.Pro295Ser
|
|
ENST00000538751.5:c.157C>T
|
ENSP00000444619.1:p.Pro53Ser
|
|
ENST00000540329.5:c.67C>T
|
ENSP00000440018.1:p.Pro23Ser
|
|
ENST00000541756.5:c.685C>T
|
ENSP00000446360.2:p.Pro229Ser
|
|
NM_001567.3:c.883C>T
|
NP_001558.3:p.Pro295Ser
|
|
XM_005273978.3:c.949C>T
|
XP_005274035.1:p.Pro317Ser
|
|
XM_005273979.3:c.949C>T
|
XP_005274036.1:p.Pro317Ser
|
|
XM_011544999.1:c.883C>T
|
XP_011543301.1:p.Pro295Ser
|
|
XM_011545000.1:c.949C>T
|
XP_011543302.1:p.Pro317Ser
|
|
XM_005273979.4:c.949C>T
|
XP_005274036.1:p.Pro317Ser
|
|
XM_011544999.2:c.883C>T
|
XP_011543301.1:p.Pro295Ser
|
|
XM_024448501.1:c.949C>T
|
XP_024304269.1:p.Pro317Ser
|
|
XM_024448502.1:c.949C>T
|
XP_024304270.1:p.Pro317Ser
|
|
XM_024448503.1:c.919C>T
|
XP_024304271.1:p.Pro307Ser
|
|
XM_024448504.1:c.883C>T
|
XP_024304272.1:p.Pro295Ser
|
|
XM_024448505.1:c.949C>T
|
XP_024304273.1:p.Pro317Ser
|
|
NM_001567.4:c.883C>T
MANE Select
|
NP_001558.3:p.Pro295Ser
|
|