ENST00000299314.12:c.3553C>T
MANE Select
|
ENSP00000299314.7:p.Pro1185Ser
|
|
ENST00000299314.11:c.3553C>T
|
ENSP00000299314.7:p.Pro1185Ser
|
|
ENST00000549738.5:c.451C>T
|
ENSP00000450161.1:n.451C>T
|
|
NM_024312.4:c.3553C>T
|
NP_077288.2:p.Pro1185Ser
|
|
XM_011538731.1:c.3472C>T
|
XP_011537033.1:p.Pro1158Ser
|
|
XM_011538731.2:c.3472C>T
|
XP_011537033.1:p.Pro1158Ser
|
|
XM_017019961.1:c.3337C>T
|
XP_016875450.1:p.Pro1113Ser
|
|
XM_017019962.2:c.2326C>T
|
XP_016875451.1:p.Pro776Ser
|
|
NM_024312.5:c.3553C>T
MANE Select
|
NP_077288.2:p.Pro1185Ser
|
|